Canonical Allele Identifier: CA1500739611
Gene:

Linked Data

dbSNP Id: rs941303441

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601663G>A , CM000666.2:g.144601663G>A GRCh38
NC_000004.11:g.145522815G>A , CM000666.1:g.145522815G>A GRCh37
NC_000004.10:g.145742265G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185685C>T ENSP00000497507.1:n.328-185685C>T