Canonical Allele Identifier: CA2015750623
Gene: CLEC12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017496C= , CM000674.2:g.10017496C= GRCh38
NC_000012.11:g.10170095C= , CM000674.1:g.10170095C= GRCh37
NC_000012.10:g.10061362C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000338896.11:c.681-835C= MANE Select ENSP00000344563.5:n.681-835C=
ENST00000338896.10:c.681-835C= ENSP00000344563.5:n.681-835C=
ENST00000338896.9:c.681-835C= ENSP00000344563.5:n.681-835C=
ENST00000396502.5:c.*1750C= ENSP00000379759.1:n.*1750C=
ENST00000539155.1:c.*2243C= ENSP00000444909.1:n.*2243C=
ENST00000544853.5:c.*129-835C= ENSP00000439561.1:n.*129-835C=
NM_001129998.1:c.681-835C= NP_001123470.1:n.681-835C=
NM_205852.2:c.*1750C= NP_995324.2:n.*1750C=
NR_120484.1:n.249-1723G=
XM_006719070.2:c.681-922C= XP_006719133.1:n.681-922C=
XM_006719071.2:c.*3-835C= XP_006719134.1:n.*3-835C=
XM_006719072.1:c.*523C= XP_006719135.1:n.*523C=
XM_011520658.1:c.654-835C= XP_011518960.1:n.654-835C=
XM_011520659.1:c.*499C= XP_011518961.1:n.*499C=
XM_011520660.1:c.*494C= XP_011518962.1:n.*494C=
XM_011520661.1:c.*10-835C= XP_011518963.1:n.*10-835C=
XM_011520662.1:c.*530C= XP_011518964.1:n.*530C=
XM_011520663.1:c.526-835C= XP_011518965.1:n.526-835C=
XM_011520664.1:c.526-922C= XP_011518966.1:n.526-922C=
XR_242889.3:n.956-835C=
XR_931290.1:n.1476C=
NM_001129998.2:c.681-835C= NP_001123470.1:n.681-835C=
NM_001319241.1:c.372-835C= NP_001306170.1:n.372-835C=
NM_001319242.1:c.*1750C= NP_001306171.1:n.*1750C=
NM_205852.3:c.*1750C= NP_995324.2:n.*1750C=
NR_135049.1:n.961-835C=
XM_011520658.2:c.654-835C= XP_011518960.1:n.654-835C=
XM_011520663.2:c.526-835C= XP_011518965.1:n.526-835C=
XM_017019295.1:c.372-835C= XP_016874784.1:n.372-835C=
XM_024448976.1:c.681-922C= XP_024304744.1:n.681-922C=
XM_024448977.1:c.*1757C= XP_024304745.1:n.*1757C=
XR_002957401.1:n.106-1348G=
NM_001129998.3:c.681-835C= MANE Select NP_001123470.1:n.681-835C=
NM_001387138.1:c.681-922C= NP_001374067.1:n.681-922C=
NR_169587.1:n.258-1348G=