Canonical Allele Identifier: CA1769199579
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130229A= , CM000670.2:g.20130229A= GRCh38
NC_000008.10:g.19987740A= , CM000670.1:g.19987740A= GRCh37
NC_000008.9:g.20032020A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949563.1:n.3408+310A=
XR_949563.2:n.3400+310A=