Linked Data
ClinVar Variation Id:
4498
ClinVar RCV Id:
RCV000004756
dbSNP Id:
rs730880270
PubMed:
PMID:11574907
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.33964017C>T , CM000667.2:g.33964017C>T | GRCh38 |
| NC_000005.9:g.33964122C>T , CM000667.1:g.33964122C>T | GRCh37 |
| NC_000005.8:g.33999879C>T | NCBI36 |
| NG_011691.2:g.25659G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296589.9:c.563-1G>A MANE Select | ENSP00000296589.4:n.563-1G>A | |
| ENST00000296589.8:c.563-1G>A | ENSP00000296589.4:n.563-1G>A | |
| ENST00000382102.7:c.563-1G>A | ENSP00000371534.3:n.563-1G>A | |
| ENST00000505056.1:n.365-1G>A | ||
| ENST00000509381.1:c.563-9513G>A | ENSP00000421100.1:n.563-9513G>A | |
| ENST00000510600.1:c.38-1G>A | ENSP00000424010.1:n.38-1G>A | |
| NM_001012509.3:c.563-1G>A | NP_001012527.1:n.563-1G>A | |
| NM_001297417.2:c.563-9513G>A | NP_001284346.2:n.563-9513G>A | |
| NM_016180.4:c.563-1G>A | NP_057264.3:n.563-1G>A | |
| XM_011514051.1:c.161-1G>A | XP_011512353.1:n.161-1G>A | |
| XM_011514052.1:c.563-1G>A | XP_011512354.1:n.563-1G>A | |
| XR_925620.1:n.1380-1G>A | ||
| NM_016180.5:c.563-1G>A MANE Select | NP_057264.4:n.563-1G>A | |
| NM_001012509.4:c.563-1G>A | NP_001012527.2:n.563-1G>A | |
| NM_001297417.3:c.563-9513G>A | NP_001284346.2:n.563-9513G>A | |
| NM_001297417.4:c.563-9513G>A | NP_001284346.2:n.563-9513G>A |