Canonical Allele Identifier: CA1740470113
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306346T= , CM000669.2:g.124306346T= GRCh38
NC_000007.13:g.123946400T= , CM000669.1:g.123946400T= GRCh37
NC_000007.12:g.123733636T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-132T=