Canonical Allele Identifier: CA1500769968
Gene:

Linked Data

dbSNP Id: rs13141641

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144585304T>A , CM000666.2:g.144585304T>A GRCh38
NC_000004.11:g.145506456T>A , CM000666.1:g.145506456T>A GRCh37
NC_000004.10:g.145725906T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-169326A>T ENSP00000497507.1:n.328-169326A>T