Canonical Allele Identifier: CA2224227949
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56610657T= , CM000678.2:g.56610657T= GRCh38
NC_000016.9:g.56644569T= , CM000678.1:g.56644569T= GRCh37
NC_000016.8:g.55202070T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933616.1:n.605+659A=