Canonical Allele Identifier: CA1392628865
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743562C= , CM000665.2:g.109743562C= GRCh38
NC_000003.11:g.109462409C= , CM000665.1:g.109462409C= GRCh37
NC_000003.10:g.110945099C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924325.1:n.142+63367C=