Canonical Allele Identifier: CA1161925215
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523575T= , CM000663.2:g.34523575T= GRCh38
NC_000001.10:g.34989176T= , CM000663.1:g.34989176T= GRCh37
NC_000001.9:g.34761763T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947171.1:n.1073+24004A=
XR_001737964.1:n.991+24004A=