Canonical Allele Identifier: CA1267947287
Gene:

Linked Data

dbSNP Id: rs1573064617

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016103C>T , CM000664.2:g.88016103C>T GRCh38
NC_000002.11:g.88315622C>T , CM000664.1:g.88315622C>T GRCh37
NC_000002.10:g.88096737C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.448C>T
XR_940336.3:n.448C>T