Canonical Allele Identifier: CA1205766087
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649591T= , CM000663.2:g.168649591T= GRCh38
NC_000001.10:g.168618829T= , CM000663.1:g.168618829T= GRCh37
NC_000001.9:g.166885453T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8316A=
XR_922259.2:n.332-8316A=