Linked Data
ClinVar Variation Id:
97106
ClinVar RCV Id:
RCV000083331
dbSNP Id:
rs72554306
PubMed:
PMID:9452049
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38367328G>T , CM000685.2:g.38367328G>T | GRCh38 |
| NC_000023.10:g.38226581G>T , CM000685.1:g.38226581G>T | GRCh37 |
| NC_000023.9:g.38111525G>T | NCBI36 |
| NG_008471.1:g.19846G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.115G>T MANE Select | ENSP00000039007.4:p.Gly39Cys | |
| ENST00000643344.1:c.115G>T | ENSP00000496606.1:p.Gly39Cys | |
| ENST00000039007.4:c.115G>T | ENSP00000039007.4:p.Gly39Cys | |
| ENST00000465127.1:c.172-298793G>T | ENSP00000417050.1:n.172-298793G>T | |
| ENST00000488812.1:n.207G>T | ||
| NM_000531.5:c.115G>T | NP_000522.3:p.Gly39Cys | |
| XM_017029556.1:c.115G>T | XP_016885045.1:p.Gly39Cys | |
| NM_000531.6:c.115G>T MANE Select | NP_000522.3:p.Gly39Cys |