Linked Data
ClinVar Variation Id:
1701351
ClinVar RCV Id:
RCV002275533
dbSNP Id:
rs2147266672
gnomAD v4:
19-11120521-A-G
MyVariant Identifiers:
chr19:g.11231197A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11120521A>G , CM000681.2:g.11120521A>G | GRCh38 |
| NC_000019.9:g.11231197A>G , CM000681.1:g.11231197A>G | GRCh37 |
| NC_000019.8:g.11092197A>G | NCBI36 |
| NG_009060.1:g.36141A>G , LRG_274:g.36141A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2397A>G | ENSP00000252444.6:p.Thr799= | |
| ENST00000559340.2:c.*208A>G | ENSP00000453696.2:n.*208A>G | |
| ENST00000560467.2:c.2019A>G | ENSP00000453513.2:p.Thr673= | |
| ENST00000558518.6:c.2139A>G MANE Select | ENSP00000454071.1:p.Thr713= | |
| ENST00000252444.9:c.2393A>G | ||
| ENST00000455727.6:c.1635A>G | ENSP00000397829.2:p.Thr545= | |
| ENST00000535915.5:c.2016A>G | ENSP00000440520.1:p.Thr672= | |
| ENST00000545707.5:c.1606+288A>G | ENSP00000437639.1:n.1606+288A>G | |
| ENST00000557933.5:c.2139A>G | ENSP00000453557.1:p.Thr713= | |
| ENST00000558013.5:c.2139A>G | ENSP00000453346.1:p.Thr713= | |
| ENST00000558518.5:c.2139A>G | ENSP00000454071.1:p.Thr713= | |
| NM_000527.4:c.2139A>G , LRG_274t1:c.2139A>G | NP_000518.1:p.Thr713= | |
| NM_001195798.1:c.2139A>G | NP_001182727.1:p.Thr713= | |
| NM_001195799.1:c.2016A>G | NP_001182728.1:p.Thr672= | |
| NM_001195800.1:c.1635A>G | NP_001182729.1:p.Thr545= | |
| NM_001195803.1:c.1606+288A>G | NP_001182732.1:n.1606+288A>G | |
| XM_011528010.1:c.2139A>G | XP_011526312.1:p.Thr713= | |
| XM_011528011.1:c.1758A>G | XP_011526313.1:p.Thr586= | |
| XR_244074.2:n.2149A>G | ||
| XM_011528010.2:c.2139A>G | XP_011526312.1:p.Thr713= | |
| XR_001753685.2:n.2256A>G | ||
| XR_001753686.2:n.2116A>G | ||
| NM_000527.5:c.2139A>G MANE Select | NP_000518.1:p.Thr713= | |
| NM_001195798.2:c.2139A>G | NP_001182727.1:p.Thr713= | |
| NM_001195799.2:c.2016A>G | NP_001182728.1:p.Thr672= | |
| NM_001195800.2:c.1635A>G | NP_001182729.1:p.Thr545= | |
| NM_001195803.2:c.1606+288A>G | NP_001182732.1:n.1606+288A>G |