Canonical Allele Identifier: CA1350283920
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207030A= , CM000665.2:g.21207030A= GRCh38
NC_000003.11:g.21248522A= , CM000665.1:g.21248522A= GRCh37
NC_000003.10:g.21223526A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3968A=
XR_940646.2:n.547-3968A=