Canonical Allele Identifier: CA107666223
Gene:

Linked Data

dbSNP Id: rs12504628

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144515172T>C , CM000666.2:g.144515172T>C GRCh38
NC_000004.11:g.145436324T>C , CM000666.1:g.145436324T>C GRCh37
NC_000004.10:g.145655774T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-99194A>G ENSP00000497507.1:n.328-99194A>G
XR_939272.1:n.179-15652A>G
XR_939273.1:n.178+46812A>G
XR_939272.2:n.523-15652A>G
XR_939273.2:n.522+46812A>G