Canonical Allele Identifier: CA1657688871
Gene:

Linked Data

dbSNP Id: rs1776570922

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450189C>G , CM000668.2:g.117450189C>G GRCh38
NC_000006.11:g.117771352C>G , CM000668.1:g.117771352C>G GRCh37
NC_000006.10:g.117878045C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116665G>C ENSP00000487717.1:n.547+116665G>C