Canonical Allele Identifier: CA1161925235
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523612C= , CM000663.2:g.34523612C= GRCh38
NC_000001.10:g.34989213C= , CM000663.1:g.34989213C= GRCh37
NC_000001.9:g.34761800C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23967G=
XR_001737964.1:n.991+23967G=