Canonical Allele Identifier: CA1392628902
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743645T= , CM000665.2:g.109743645T= GRCh38
NC_000003.11:g.109462492T= , CM000665.1:g.109462492T= GRCh37
NC_000003.10:g.110945182T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63450T=