Canonical Allele Identifier: CA1205765948
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649252C= , CM000663.2:g.168649252C= GRCh38
NC_000001.10:g.168618490C= , CM000663.1:g.168618490C= GRCh37
NC_000001.9:g.166885114C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7977G=
XR_922259.2:n.332-7977G=