Linked Data
ClinVar Variation Id:
204082
ClinVar RCV Id:
RCV000186288
dbSNP Id:
rs180177184
PubMed:
PMID:24934730
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869246C>A , CM000664.2:g.240869246C>A | GRCh38 |
| NC_000002.11:g.241808663C>A , CM000664.1:g.241808663C>A | GRCh37 |
| NC_000002.10:g.241457336C>A | NCBI36 |
| NG_008005.1:g.5502C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.242C>A MANE Select | ENSP00000302620.3:p.Ser81Ter | |
| ENST00000307503.3:c.242C>A | ENSP00000302620.3:p.Ser81Ter | |
| ENST00000472436.1:n.262C>A | ||
| NM_000030.2:c.242C>A | NP_000021.1:p.Ser81Ter | |
| XR_924060.1:n.405+987G>T | ||
| NM_000030.3:c.242C>A MANE Select | NP_000021.1:p.Ser81Ter |