Canonical Allele Identifier: CA1350284094
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207191C= , CM000665.2:g.21207191C= GRCh38
NC_000003.11:g.21248683C= , CM000665.1:g.21248683C= GRCh37
NC_000003.10:g.21223687C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3807C=
XR_940646.2:n.547-3807C=