Canonical Allele Identifier: CA1350284071
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207168T= , CM000665.2:g.21207168T= GRCh38
NC_000003.11:g.21248660T= , CM000665.1:g.21248660T= GRCh37
NC_000003.10:g.21223664T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940646.1:n.254-3830T=
XR_940646.2:n.547-3830T=