Linked Data
ClinVar Variation Id:
361723
dbSNP Id:
rs886062653
gnomAD v3:
8-125063585-G-T
gnomAD v4:
8-125063585-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.125063585G>T , CM000670.2:g.125063585G>T | GRCh38 |
| NC_000008.10:g.126075827G>T , CM000670.1:g.126075827G>T | GRCh37 |
| NC_000008.9:g.126145009G>T | NCBI36 |
| NG_012636.1:g.33235C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318410.12:c.1345C>A MANE Select | ENSP00000318016.7:p.Arg449= | |
| ENST00000318410.11:c.1345C>A | ENSP00000318016.7:p.Arg449= | |
| ENST00000517845.5:c.901C>A | ENSP00000429676.1:p.Arg301= | |
| NM_014846.3:c.1345C>A | NP_055661.3:p.Arg449= | |
| XM_005251120.2:c.901C>A | XP_005251177.1:p.Arg301= | |
| XM_011517409.1:c.1345C>A | XP_011515711.1:p.Arg449= | |
| XM_011517410.1:c.1345C>A | XP_011515712.1:p.Arg449= | |
| NM_001330609.1:c.901C>A | NP_001317538.1:p.Arg301= | |
| XM_017014113.2:c.1345C>A | XP_016869602.1:p.Arg449= | |
| NM_014846.4:c.1345C>A MANE Select | NP_055661.3:p.Arg449= | |
| NM_001330609.2:c.901C>A | NP_001317538.1:p.Arg301= |