Canonical Allele Identifier: CA232780615
Gene: CLEC12B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11053548

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10018128A>G , CM000674.2:g.10018128A>G GRCh38
NC_000012.11:g.10170727A>G , CM000674.1:g.10170727A>G GRCh37
NC_000012.10:g.10061994A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001129998.1:c.681-203A>G VV NP_001123470.1:p.=
NR_120484.1:n.249-2355T>C
XM_006719070.2:c.681-290A>G XP_006719133.1:p.=
XM_006719071.2:c.*3-203A>G XP_006719134.1:p.=
XM_011520658.1:c.654-203A>G XP_011518960.1:p.=
XM_011520661.1:c.*10-203A>G XP_011518963.1:p.=
XM_011520663.1:c.526-203A>G XP_011518965.1:p.=
XM_011520664.1:c.526-290A>G XP_011518966.1:p.=
XR_242889.3:n.956-203A>G
NM_001129998.2:c.681-203A>G VV
NM_001319241.1:c.372-203A>G VV NP_001306170.1:p.=
NR_135049.1:n.961-203A>G
XM_011520658.2:c.654-203A>G
XM_011520663.2:c.526-203A>G
XM_017019295.1:c.372-203A>G XP_016874784.1:p.=
XM_024448976.1:c.681-290A>G XP_024304744.1:p.=
XR_002957401.1:n.106-1980T>C
ENST00000338896.9:c.681-203A>G ENSP00000344563.5:p.=
ENST00000544853.5:c.*129-203A>G ENSP00000439561.1:p.=