Canonical Allele Identifier: CA1140847064
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649216C= , CM000663.2:g.168649216C= GRCh38
NC_000001.10:g.168618454C= , CM000663.1:g.168618454C= GRCh37
NC_000001.9:g.166885078C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7941G=
XR_922259.2:n.332-7941G=