Canonical Allele Identifier: CA2512296784
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787721G>A , CM000671.2:g.1787721G>A GRCh38
NC_000009.11:g.1787721G>A , CM000671.1:g.1787721G>A GRCh37
NC_000009.10:g.1777721G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68809G>A