Canonical Allele Identifier: CA1392628842
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743489A= , CM000665.2:g.109743489A= GRCh38
NC_000003.11:g.109462336A= , CM000665.1:g.109462336A= GRCh37
NC_000003.10:g.110945026A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63294A=