Canonical Allele Identifier: CA2008287866
Gene:

Linked Data

dbSNP Id: rs881333

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870788C>T , CM000673.2:g.128870788C>T GRCh38
NC_000011.9:g.128740683C>T , CM000673.1:g.128740683C>T GRCh37
NC_000011.8:g.128245893C>T NCBI36
NG_009379.1:g.1586G>A

Transcript Alleles

HGVS Amino-acid change
XR_948172.1:n.6123G>A
XR_948173.1:n.5812G>A