Linked Data
ClinVar Variation Id:
344266
dbSNP Id:
rs376737530
ExAC:
3:180359927 G / A
gnomAD v2:
3-180359927-G-A
gnomAD v3:
3-180642139-G-A
gnomAD v4:
3-180642139-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180642139G>A , CM000665.2:g.180642139G>A | GRCh38 |
| NC_000003.11:g.180359927G>A , CM000665.1:g.180359927G>A | GRCh37 |
| NC_000003.10:g.181842621G>A | NCBI36 |
| NG_029581.1:g.42357C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.1728C>T MANE Select | ENSP00000417960.2:p.His576= | |
| ENST00000650641.1:n.1615C>T | ||
| ENST00000651046.1:c.1536C>T | ENSP00000499175.1:p.His512= | |
| ENST00000651922.1:n.1053C>T | ||
| ENST00000652408.1:n.1865C>T | ||
| ENST00000442201.6:c.1728C>T | ENSP00000405708.2:p.His576= | |
| ENST00000476379.5:c.1728C>T | ENSP00000417960.1:p.His576= | |
| NM_181426.1:c.1728C>T | NP_852091.1:p.His576= | |
| NM_181426.2:c.1728C>T MANE Select | NP_852091.1:p.His576= |