Canonical Allele Identifier: CA894254280
Gene:

Linked Data

dbSNP Id: rs1421996703

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016192G>T , CM000664.2:g.88016192G>T GRCh38
NC_000002.11:g.88315711G>T , CM000664.1:g.88315711G>T GRCh37
NC_000002.10:g.88096826G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.537G>T
XR_940336.3:n.537G>T