Canonical Allele Identifier: CA1657688879
Gene:

Linked Data

dbSNP Id: rs1776571028

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450202C>A , CM000668.2:g.117450202C>A GRCh38
NC_000006.11:g.117771365C>A , CM000668.1:g.117771365C>A GRCh37
NC_000006.10:g.117878058C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116652G>T ENSP00000487717.1:n.547+116652G>T