Canonical Allele Identifier: CA1657688813
Gene:

Linked Data

dbSNP Id: rs1776568744

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450053T>G , CM000668.2:g.117450053T>G GRCh38
NC_000006.11:g.117771216T>G , CM000668.1:g.117771216T>G GRCh37
NC_000006.10:g.117877909T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116801A>C ENSP00000487717.1:n.547+116801A>C