Canonical Allele Identifier: CA1161925228
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523591A= , CM000663.2:g.34523591A= GRCh38
NC_000001.10:g.34989192A= , CM000663.1:g.34989192A= GRCh37
NC_000001.9:g.34761779A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23988T=
XR_001737964.1:n.991+23988T=