Canonical Allele Identifier: CA2008287932
Gene:

Linked Data

dbSNP Id: rs1943912158

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870962C>T , CM000673.2:g.128870962C>T GRCh38
NC_000011.9:g.128740857C>T , CM000673.1:g.128740857C>T GRCh37
NC_000011.8:g.128246067C>T NCBI36
NG_009379.1:g.1412G>A

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5949G>A
XR_948173.1:n.5638G>A