Linked Data
ClinVar Variation Id:
16472
ClinVar RCV Id:
RCV000017936
dbSNP Id:
rs267606801
PubMed:
PMID:11700157
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48467956A>C , CM000677.2:g.48467956A>C | GRCh38 |
| NC_000015.9:g.48760153A>C , CM000677.1:g.48760153A>C | GRCh37 |
| NC_000015.8:g.46547445A>C | NCBI36 |
| NG_008805.2:g.182833T>G , LRG_778:g.182833T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559133.6:c.4729T>G | ENSP00000453958.2:p.Cys1577Gly | |
| ENST00000674301.2:c.4729T>G | ENSP00000501333.2:p.Cys1577Gly | |
| ENST00000684448.1:n.3403T>G | ||
| ENST00000316623.10:c.4729T>G MANE Select | ENSP00000325527.5:p.Cys1577Gly | |
| ENST00000316623.9:c.4729T>G | ENSP00000325527.5:p.Cys1577Gly | |
| ENST00000537463.6:c.*492T>G | ENSP00000440294.2:n.*492T>G | |
| ENST00000559133.5:c.36T>G | ||
| NM_000138.4:c.4729T>G , LRG_778t1:c.4729T>G | NP_000129.3:p.Cys1577Gly | |
| NM_000138.5:c.4729T>G MANE Select | NP_000129.3:p.Cys1577Gly |