Canonical Allele Identifier: CA1392628828
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743430A= , CM000665.2:g.109743430A= GRCh38
NC_000003.11:g.109462277A= , CM000665.1:g.109462277A= GRCh37
NC_000003.10:g.110944967A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63235A=