Linked Data
ClinVar Variation Id:
1598478
ClinVar RCV Id:
RCV002122562
dbSNP Id:
rs1260214548
gnomAD v4:
5-173233135-G-T
MyVariant Identifiers:
chr5:g.172660138G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173233135G>T , CM000667.2:g.173233135G>T | GRCh38 |
| NC_000005.9:g.172660138G>T , CM000667.1:g.172660138G>T | GRCh37 |
| NC_000005.8:g.172592744G>T | NCBI36 |
| NG_013340.1:g.7178C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.409C>A MANE Select | ENSP00000327758.4:p.Arg137= | |
| ENST00000329198.4:c.409C>A | ENSP00000327758.4:p.Arg137= | |
| ENST00000424406.2:c.*362C>A | ENSP00000395378.2:n.*362C>A | |
| ENST00000521848.1:c.*208C>A | ENSP00000427906.1:n.*208C>A | |
| NM_001166175.1:c.*362C>A | NP_001159647.1:n.*362C>A | |
| NM_001166176.1:c.*208C>A | NP_001159648.1:n.*208C>A | |
| NM_004387.3:c.409C>A | NP_004378.1:p.Arg137= | |
| NM_004387.4:c.409C>A MANE Select | NP_004378.1:p.Arg137= | |
| NM_001166175.2:c.*362C>A | NP_001159647.1:n.*362C>A | |
| NM_001166176.2:c.*208C>A | NP_001159648.1:n.*208C>A |