Linked Data
dbSNP Id:
rs1357796003
gnomAD v2:
19-48922922-G-A
gnomAD v3:
19-48419665-G-A
gnomAD v4:
19-48419665-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48419665G>A , CM000681.2:g.48419665G>A | GRCh38 |
| NC_000019.9:g.48922922G>A , CM000681.1:g.48922922G>A | GRCh37 |
| NC_000019.8:g.53614734G>A | NCBI36 |
| NG_052829.1:g.29791G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263269.4:c.1942G>A MANE Select | ENSP00000263269.2:p.Glu648Lys | |
| ENST00000263269.3:c.1942G>A | ENSP00000263269.2:p.Glu648Lys | |
| NM_000836.2:c.1942G>A | NP_000827.2:p.Glu648Lys | |
| XM_011526872.1:c.1942G>A | XP_011525174.1:p.Glu648Lys | |
| NM_000836.4:c.1942G>A MANE Select | NP_000827.2:p.Glu648Lys |