Canonical Allele Identifier: CA1841175634
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551515G= , CM000671.2:g.25551515G= GRCh38
NC_000009.11:g.25551513G= , CM000671.1:g.25551513G= GRCh37
NC_000009.10:g.25541513G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-943C=
XR_929525.2:n.674-943C=