Canonical Allele Identifier: CA2015750779
Gene: CLEC12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017875T= , CM000674.2:g.10017875T= GRCh38
NC_000012.11:g.10170474T= , CM000674.1:g.10170474T= GRCh37
NC_000012.10:g.10061741T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338896.11:c.681-456T= MANE Select ENSP00000344563.5:n.681-456T=
ENST00000338896.10:c.681-456T= ENSP00000344563.5:n.681-456T=
ENST00000338896.9:c.681-456T= ENSP00000344563.5:n.681-456T=
ENST00000396502.5:c.*2129T= ENSP00000379759.1:n.*2129T=
ENST00000539155.1:c.*2622T= ENSP00000444909.1:n.*2622T=
ENST00000544853.5:c.*129-456T= ENSP00000439561.1:n.*129-456T=
NM_001129998.1:c.681-456T= NP_001123470.1:n.681-456T=
NM_205852.2:c.*2129T= NP_995324.2:n.*2129T=
NR_120484.1:n.249-2102A=
XM_006719070.2:c.681-543T= XP_006719133.1:n.681-543T=
XM_006719071.2:c.*3-456T= XP_006719134.1:n.*3-456T=
XM_006719072.1:c.*902T= XP_006719135.1:n.*902T=
XM_011520658.1:c.654-456T= XP_011518960.1:n.654-456T=
XM_011520659.1:c.*878T= XP_011518961.1:n.*878T=
XM_011520660.1:c.*873T= XP_011518962.1:n.*873T=
XM_011520661.1:c.*10-456T= XP_011518963.1:n.*10-456T=
XM_011520662.1:c.*909T= XP_011518964.1:n.*909T=
XM_011520663.1:c.526-456T= XP_011518965.1:n.526-456T=
XM_011520664.1:c.526-543T= XP_011518966.1:n.526-543T=
XR_242889.3:n.956-456T=
XR_931290.1:n.1855T=
NM_001129998.2:c.681-456T= NP_001123470.1:n.681-456T=
NM_001319241.1:c.372-456T= NP_001306170.1:n.372-456T=
NM_001319242.1:c.*2129T= NP_001306171.1:n.*2129T=
NM_205852.3:c.*2129T= NP_995324.2:n.*2129T=
NR_135049.1:n.961-456T=
XM_011520658.2:c.654-456T= XP_011518960.1:n.654-456T=
XM_011520663.2:c.526-456T= XP_011518965.1:n.526-456T=
XM_017019295.1:c.372-456T= XP_016874784.1:n.372-456T=
XM_024448976.1:c.681-543T= XP_024304744.1:n.681-543T=
XM_024448977.1:c.*2136T= XP_024304745.1:n.*2136T=
XR_002957401.1:n.106-1727A=
NM_001129998.3:c.681-456T= MANE Select NP_001123470.1:n.681-456T=
NM_001387138.1:c.681-543T= NP_001374067.1:n.681-543T=
NR_169587.1:n.258-1727A=