Canonical Allele Identifier: CA1740470108
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306338T= , CM000669.2:g.124306338T= GRCh38
NC_000007.13:g.123946392T= , CM000669.1:g.123946392T= GRCh37
NC_000007.12:g.123733628T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-140T=