Canonical Allele Identifier: CA1392628830
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743443T= , CM000665.2:g.109743443T= GRCh38
NC_000003.11:g.109462290T= , CM000665.1:g.109462290T= GRCh37
NC_000003.10:g.110944980T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63248T=