Canonical Allele Identifier: CA1350284000
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207110C= , CM000665.2:g.21207110C= GRCh38
NC_000003.11:g.21248602C= , CM000665.1:g.21248602C= GRCh37
NC_000003.10:g.21223606C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3888C=
XR_940646.2:n.547-3888C=