Canonical Allele Identifier: CA646808066
Gene:

Linked Data

dbSNP Id: rs1672662820

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015866G>T , CM000664.2:g.88015866G>T GRCh38
NC_000002.11:g.88315385G>T , CM000664.1:g.88315385G>T GRCh37
NC_000002.10:g.88096500G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.211G>T
XR_940336.3:n.211G>T