Canonical Allele Identifier: CA1224246984
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887030T= , CM000663.2:g.224887030T= GRCh38
NC_000001.10:g.225074732T= , CM000663.1:g.225074732T= GRCh37
NC_000001.9:g.223141355T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2249A=
XR_949207.2:n.63-2249A=