Canonical Allele Identifier: CA2015750613
Gene: CLEC12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017469C= , CM000674.2:g.10017469C= GRCh38
NC_000012.11:g.10170068C= , CM000674.1:g.10170068C= GRCh37
NC_000012.10:g.10061335C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000338896.11:c.681-862C= MANE Select ENSP00000344563.5:n.681-862C=
ENST00000338896.10:c.681-862C= ENSP00000344563.5:n.681-862C=
ENST00000338896.9:c.681-862C= ENSP00000344563.5:n.681-862C=
ENST00000396502.5:c.*1723C= ENSP00000379759.1:n.*1723C=
ENST00000539155.1:c.*2216C= ENSP00000444909.1:n.*2216C=
ENST00000544853.5:c.*129-862C= ENSP00000439561.1:n.*129-862C=
NM_001129998.1:c.681-862C= NP_001123470.1:n.681-862C=
NM_205852.2:c.*1723C= NP_995324.2:n.*1723C=
NR_120484.1:n.249-1696G=
XM_006719070.2:c.681-949C= XP_006719133.1:n.681-949C=
XM_006719071.2:c.*3-862C= XP_006719134.1:n.*3-862C=
XM_006719072.1:c.*496C= XP_006719135.1:n.*496C=
XM_011520658.1:c.654-862C= XP_011518960.1:n.654-862C=
XM_011520659.1:c.*472C= XP_011518961.1:n.*472C=
XM_011520660.1:c.*467C= XP_011518962.1:n.*467C=
XM_011520661.1:c.*10-862C= XP_011518963.1:n.*10-862C=
XM_011520662.1:c.*503C= XP_011518964.1:n.*503C=
XM_011520663.1:c.526-862C= XP_011518965.1:n.526-862C=
XM_011520664.1:c.526-949C= XP_011518966.1:n.526-949C=
XR_242889.3:n.956-862C=
XR_931290.1:n.1449C=
NM_001129998.2:c.681-862C= NP_001123470.1:n.681-862C=
NM_001319241.1:c.372-862C= NP_001306170.1:n.372-862C=
NM_001319242.1:c.*1723C= NP_001306171.1:n.*1723C=
NM_205852.3:c.*1723C= NP_995324.2:n.*1723C=
NR_135049.1:n.961-862C=
XM_011520658.2:c.654-862C= XP_011518960.1:n.654-862C=
XM_011520663.2:c.526-862C= XP_011518965.1:n.526-862C=
XM_017019295.1:c.372-862C= XP_016874784.1:n.372-862C=
XM_024448976.1:c.681-949C= XP_024304744.1:n.681-949C=
XM_024448977.1:c.*1730C= XP_024304745.1:n.*1730C=
XR_002957401.1:n.106-1321G=
NM_001129998.3:c.681-862C= MANE Select NP_001123470.1:n.681-862C=
NM_001387138.1:c.681-949C= NP_001374067.1:n.681-949C=
NR_169587.1:n.258-1321G=