Canonical Allele Identifier: CA1392628816
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743395G= , CM000665.2:g.109743395G= GRCh38
NC_000003.11:g.109462242G= , CM000665.1:g.109462242G= GRCh37
NC_000003.10:g.110944932G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63200G=