Linked Data
dbSNP Id:
rs942895422
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122460990C>T , CM000672.2:g.122460990C>T | GRCh38 |
| NC_000010.10:g.124220506C>T , CM000672.1:g.124220506C>T | GRCh37 |
| NC_000010.9:g.124210496C>T | NCBI36 |
| NG_011554.1:g.4466C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000648167.1:c.154+2281C>T | ENSP00000498033.1:n.154+2281C>T | |
| XR_946382.1:n.369G>A | ||
| XR_946383.1:n.369G>A | ||
| XR_946384.1:n.369G>A | ||
| XR_946385.1:n.369G>A | ||
| XR_946382.2:n.397G>A | ||
| XR_946383.2:n.397G>A | ||
| XR_946384.2:n.373G>A | ||
| XR_946385.2:n.397G>A |