Canonical Allele Identifier: CA1205766022
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649436G= , CM000663.2:g.168649436G= GRCh38
NC_000001.10:g.168618674G= , CM000663.1:g.168618674G= GRCh37
NC_000001.9:g.166885298G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8161C=
XR_922259.2:n.332-8161C=