Linked Data
ClinVar Variation Id:
13227
ClinVar RCV Id:
RCV000014131
dbSNP Id:
rs121918558
gnomAD v4:
3-165830567-T-C
COSMIC:
COSM4801297
PubMed:
PMID:9543549
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165830567T>C , CM000665.2:g.165830567T>C | GRCh38 |
| NC_000003.11:g.165548355T>C , CM000665.1:g.165548355T>C | GRCh37 |
| NC_000003.10:g.167031049T>C | NCBI36 |
| NG_009031.1:g.11899A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264381.8:c.467A>G MANE Select | ENSP00000264381.3:p.Tyr156Cys | |
| ENST00000264381.7:c.467A>G | ENSP00000264381.3:p.Tyr156Cys | |
| ENST00000479451.5:c.107+6747A>G | ENSP00000418325.1:n.107+6747A>G | |
| ENST00000482958.1:c.467A>G | ENSP00000419804.1:p.Tyr156Cys | |
| ENST00000488954.1:c.107+6747A>G | ENSP00000418504.1:n.107+6747A>G | |
| ENST00000497011.5:c.467A>G | ENSP00000419505.1:p.Tyr156Cys | |
| NM_000055.2:c.467A>G | NP_000046.1:p.Tyr156Cys | |
| XM_005247685.1:c.590A>G | XP_005247742.1:p.Tyr197Cys | |
| NM_000055.3:c.467A>G | NP_000046.1:p.Tyr156Cys | |
| NR_137635.1:n.159+6747A>G | ||
| NR_137636.1:n.634A>G | ||
| NM_000055.4:c.467A>G MANE Select | NP_000046.1:p.Tyr156Cys | |
| NR_137635.2:n.110+6747A>G | ||
| NR_137636.2:n.585A>G |