Canonical Allele Identifier: CA1161925236
Gene:

Linked Data

dbSNP Id: rs1639364006

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523615G>A , CM000663.2:g.34523615G>A GRCh38
NC_000001.10:g.34989216G>A , CM000663.1:g.34989216G>A GRCh37
NC_000001.9:g.34761803G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23964C>T
XR_001737964.1:n.991+23964C>T