Linked Data
ClinVar Variation Id:
938
dbSNP Id:
rs72555365
gnomAD v2:
3-33058236-G-A
gnomAD v3:
3-33016744-G-A
gnomAD v4:
3-33016744-G-A
PubMed:
PMID:7586649
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33016744G>A , CM000665.2:g.33016744G>A | GRCh38 |
| NC_000003.11:g.33058236G>A , CM000665.1:g.33058236G>A | GRCh37 |
| NC_000003.10:g.33033240G>A | NCBI36 |
| NG_009005.1:g.85459C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.1444C>T MANE Select | ENSP00000306920.4:p.Arg482Cys | |
| ENST00000307363.9:c.1444C>T | ENSP00000306920.4:p.Arg482Cys | |
| ENST00000307377.12:c.1051C>T | ENSP00000305920.8:p.Arg351Cys | |
| ENST00000399402.7:c.1354C>T | ENSP00000382333.2:p.Arg452Cys | |
| ENST00000461475.5:n.543C>T | ||
| ENST00000467571.5:n.481C>T | ||
| ENST00000497796.5:n.696C>T | ||
| NM_000404.2:c.1444C>T | NP_000395.2:p.Arg482Cys | |
| NM_000404.3:c.1444C>T | NP_000395.2:p.Arg482Cys | |
| NM_001079811.1:c.1354C>T | NP_001073279.1:p.Arg452Cys | |
| NM_001079811.2:c.1354C>T | NP_001073279.1:p.Arg452Cys | |
| NM_001135602.1:c.1051C>T | NP_001129074.1:p.Arg351Cys | |
| NM_001135602.2:c.1051C>T | NP_001129074.1:p.Arg351Cys | |
| NM_001317040.1:c.1588C>T | NP_001303969.1:p.Arg530Cys | |
| NM_000404.4:c.1444C>T MANE Select | NP_000395.3:p.Arg482Cys | |
| NM_001079811.3:c.1354C>T | NP_001073279.2:p.Arg452Cys | |
| NM_001135602.3:c.1051C>T | NP_001129074.2:p.Arg351Cys | |
| NM_001317040.2:c.1588C>T | NP_001303969.2:p.Arg530Cys | |
| NM_001393580.1:c.1444C>T | NP_001380509.1:p.Arg482Cys |