Canonical Allele Identifier: CA1205765917
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649175C= , CM000663.2:g.168649175C= GRCh38
NC_000001.10:g.168618413C= , CM000663.1:g.168618413C= GRCh37
NC_000001.9:g.166885037C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7900G=
XR_922259.2:n.332-7900G=