Linked Data
ClinVar Variation Id:
471974
ClinVar RCV Id:
RCV002395436
dbSNP Id:
rs746359389
ExAC:
7:128480091 G / T
gnomAD v2:
7-128480091-G-T
gnomAD v3:
7-128840037-G-T
gnomAD v4:
7-128840037-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128840037G>T , CM000669.2:g.128840037G>T | GRCh38 |
| NC_000007.13:g.128480091G>T , CM000669.1:g.128480091G>T | GRCh37 |
| NC_000007.12:g.128267327G>T | NCBI36 |
| NG_011807.1:g.14609G>T , LRG_870:g.14609G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.1426G>T MANE Select | ENSP00000327145.8:p.Ala476Ser | |
| ENST00000325888.12:c.1426G>T | ENSP00000327145.8:p.Ala476Ser | |
| ENST00000346177.6:c.1426G>T | ENSP00000344002.6:p.Ala476Ser | |
| NM_001127487.1:c.1426G>T | NP_001120959.1:p.Ala476Ser | |
| NM_001458.4:c.1426G>T , LRG_870t1:c.1426G>T | NP_001449.3:p.Ala476Ser | |
| NM_001127487.2:c.1426G>T | NP_001120959.1:p.Ala476Ser | |
| NM_001458.5:c.1426G>T MANE Select | NP_001449.3:p.Ala476Ser |