Canonical Allele Identifier: CA2224227959
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56610677T= , CM000678.2:g.56610677T= GRCh38
NC_000016.9:g.56644589T= , CM000678.1:g.56644589T= GRCh37
NC_000016.8:g.55202090T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933616.1:n.605+639A=