Linked Data
ClinVar Variation Id:
12863
ClinVar RCV Id:
RCV000013723
dbSNP Id:
rs754614154
PubMed:
PMID:8941647
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.158636763T>C , CM000663.2:g.158636763T>C | GRCh38 |
| NC_000001.10:g.158606553T>C , CM000663.1:g.158606553T>C | GRCh37 |
| NC_000001.9:g.156873177T>C | NCBI36 |
| NG_011474.1:g.54954A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643759.2:c.5190-2A>G MANE Select | ENSP00000495214.1:n.5190-2A>G | |
| ENST00000368147.8:c.5190-2A>G | ENSP00000357129.4:n.5190-2A>G | |
| ENST00000614909.4:c.5190-2A>G | ENSP00000482595.1:n.5190-2A>G | |
| NM_003126.2:c.5190-2A>G | NP_003117.2:n.5190-2A>G | |
| XM_011509916.1:c.5190-2A>G | XP_011508218.1:n.5190-2A>G | |
| XM_011509917.1:c.5190-2A>G | XP_011508219.1:n.5190-2A>G | |
| XM_011509918.1:c.5190-2A>G | XP_011508220.1:n.5190-2A>G | |
| XM_011509919.1:c.4981-2A>G | XP_011508221.1:n.4981-2A>G | |
| XR_921911.1:n.5303-2A>G | ||
| NM_003126.3:c.5190-2A>G | NP_003117.2:n.5190-2A>G | |
| XM_011509916.2:c.5190-2A>G | XP_011508218.1:n.5190-2A>G | |
| XM_011509917.3:c.5190-2A>G | XP_011508219.1:n.5190-2A>G | |
| XM_011509918.3:c.5190-2A>G | XP_011508220.1:n.5190-2A>G | |
| XM_011509919.3:c.4981-2A>G | XP_011508221.1:n.4981-2A>G | |
| XR_921911.3:n.5316-2A>G | ||
| NM_003126.4:c.5190-2A>G MANE Select | NP_003117.2:n.5190-2A>G |