Canonical Allele Identifier: CA2786053992
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576795A>G , CM000671.2:g.129576795A>G GRCh38
NC_000009.11:g.132339074A>G , CM000671.1:g.132339074A>G GRCh37
NC_000009.10:g.131378895A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1197A>G