Canonical Allele Identifier: CA1205766028
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649443C= , CM000663.2:g.168649443C= GRCh38
NC_000001.10:g.168618681C= , CM000663.1:g.168618681C= GRCh37
NC_000001.9:g.166885305C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8168G=
XR_922259.2:n.332-8168G=