Canonical Allele Identifier: CA479932808
Gene: TARBP2 HGNC NCBI
MAP3K12 HGNC NCBI

Linked Data

dbSNP Id: rs784567
MyVariant Identifiers: chr12:g.53894465G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53500681G>C , CM000674.2:g.53500681G>C GRCh38
NC_000012.11:g.53894465G>C , CM000674.1:g.53894465G>C GRCh37
NC_000012.10:g.52180732G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005269120.3:c.-1143G>C (TARBP2) XP_005269177.1:n.-1143G>C
XM_011538725.3:c.-691C>G (MAP3K12) XP_011537027.1:n.-691C>G