Canonical Allele Identifier: CA1161925232
Gene:

Linked Data

dbSNP Id: rs867415158

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523600C>T , CM000663.2:g.34523600C>T GRCh38
NC_000001.10:g.34989201C>T , CM000663.1:g.34989201C>T GRCh37
NC_000001.9:g.34761788C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23979G>A
XR_001737964.1:n.991+23979G>A