Canonical Allele Identifier:
CA1500737909
Gene:
Linked Data
dbSNP Id:
rs571338231
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144559616G>A , CM000666.2:g.144559616G>A | GRCh38 |
| NC_000004.11:g.145480768G>A , CM000666.1:g.145480768G>A | GRCh37 |
| NC_000004.10:g.145700218G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-143638C>T | ENSP00000497507.1:n.328-143638C>T | |
| XR_939272.1:n.178+2368C>T | ||
| XR_939273.1:n.178+2368C>T | ||
| XR_939272.2:n.522+2368C>T | ||
| XR_939273.2:n.522+2368C>T |