Linked Data
ClinVar Variation Id:
767212
dbSNP Id:
rs774883359
ExAC:
19:18267018 A / G
gnomAD v2:
19-18267018-A-G
gnomAD v3:
19-18156208-A-G
gnomAD v4:
19-18156208-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18156208A>G , CM000681.2:g.18156208A>G | GRCh38 |
| NC_000019.9:g.18267018A>G , CM000681.1:g.18267018A>G | GRCh37 |
| NC_000019.8:g.18128018A>G | NCBI36 |
| NG_033010.1:g.8031A>G | |
| NG_033010.2:g.8031A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222254.13:c.322+7A>G MANE Select | ENSP00000222254.6:n.322+7A>G | |
| ENST00000617130.5:c.322+7A>G | ENSP00000477864.2:n.322+7A>G | |
| ENST00000617642.2:c.322+7A>G | ENSP00000484714.2:n.322+7A>G | |
| ENST00000222254.12:c.322+7A>G | ENSP00000222254.6:n.322+7A>G | |
| ENST00000426902.5:c.322+7A>G | ENSP00000395636.1:n.322+7A>G | |
| ENST00000593731.1:c.322+7A>G | ENSP00000471914.1:n.322+7A>G | |
| ENST00000617130.4:c.322+7A>G | ENSP00000477864.1:n.322+7A>G | |
| ENST00000617642.1:c.322+7A>G | ENSP00000484714.1:n.322+7A>G | |
| NM_005027.3:c.322+7A>G | NP_005018.1:n.322+7A>G | |
| NR_073517.1:n.862+7A>G | ||
| NM_005027.4:c.322+7A>G MANE Select | NP_005018.2:n.322+7A>G | |
| NR_073517.2:n.877+7A>G | ||
| NR_162071.1:n.877+7A>G |