Canonical Allele Identifier: CA1350284092
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207186G= , CM000665.2:g.21207186G= GRCh38
NC_000003.11:g.21248678G= , CM000665.1:g.21248678G= GRCh37
NC_000003.10:g.21223682G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940646.1:n.254-3812G=
XR_940646.2:n.547-3812G=