Linked Data
dbSNP Id:
rs191859969
gnomAD v4:
19-11111745-G-T
MyVariant Identifiers:
chr19:g.11111745G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11111745G>T , CM000681.2:g.11111745G>T | GRCh38 |
| NC_000019.9:g.11222421G>T , CM000681.1:g.11222421G>T | GRCh37 |
| NC_000019.8:g.11083421G>T | NCBI36 |
| NG_009060.1:g.27365G>T , LRG_274:g.27365G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1444+106G>T | ENSP00000252444.6:n.1444+106G>T | |
| ENST00000559340.2:c.1186+106G>T | ENSP00000453696.2:n.1186+106G>T | |
| ENST00000560467.2:c.1066+106G>T | ENSP00000453513.2:n.1066+106G>T | |
| ENST00000558518.6:c.1186+106G>T MANE Select | ENSP00000454071.1:n.1186+106G>T | |
| ENST00000252444.9:c.1440+106G>T | ||
| ENST00000455727.6:c.682+106G>T | ENSP00000397829.2:n.682+106G>T | |
| ENST00000535915.5:c.1063+106G>T | ENSP00000440520.1:n.1063+106G>T | |
| ENST00000545707.5:c.805+106G>T | ENSP00000437639.1:n.805+106G>T | |
| ENST00000557933.5:c.1186+106G>T | ENSP00000453557.1:n.1186+106G>T | |
| ENST00000558013.5:c.1186+106G>T | ENSP00000453346.1:n.1186+106G>T | |
| ENST00000558518.5:c.1186+106G>T | ENSP00000454071.1:n.1186+106G>T | |
| ENST00000560173.1:n.185+106G>T | ||
| ENST00000560467.1:c.666+106G>T | ||
| NM_000527.4:c.1186+106G>T , LRG_274t1:c.1186+106G>T | NP_000518.1:n.1186+106G>T | |
| NM_001195798.1:c.1186+106G>T | NP_001182727.1:n.1186+106G>T | |
| NM_001195799.1:c.1063+106G>T | NP_001182728.1:n.1063+106G>T | |
| NM_001195800.1:c.682+106G>T | NP_001182729.1:n.682+106G>T | |
| NM_001195803.1:c.805+106G>T | NP_001182732.1:n.805+106G>T | |
| XM_011528010.1:c.1186+106G>T | XP_011526312.1:n.1186+106G>T | |
| XM_011528011.1:c.805+106G>T | XP_011526313.1:n.805+106G>T | |
| XR_244074.2:n.1336+106G>T | ||
| XM_011528010.2:c.1186+106G>T | XP_011526312.1:n.1186+106G>T | |
| XR_001753685.2:n.1303+106G>T | ||
| XR_001753686.2:n.1303+106G>T | ||
| NM_000527.5:c.1186+106G>T MANE Select | NP_000518.1:n.1186+106G>T | |
| NM_001195798.2:c.1186+106G>T | NP_001182727.1:n.1186+106G>T | |
| NM_001195799.2:c.1063+106G>T | NP_001182728.1:n.1063+106G>T | |
| NM_001195800.2:c.682+106G>T | NP_001182729.1:n.682+106G>T | |
| NM_001195803.2:c.805+106G>T | NP_001182732.1:n.805+106G>T |