Canonical Allele Identifier: CA1267947268
Gene:

Linked Data

dbSNP Id: rs1672672646

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016084A>T , CM000664.2:g.88016084A>T GRCh38
NC_000002.11:g.88315603A>T , CM000664.1:g.88315603A>T GRCh37
NC_000002.10:g.88096718A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.429A>T
XR_940336.3:n.429A>T