Canonical Allele Identifier: CA2794520264
Gene: CLEC12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017856A>T , CM000674.2:g.10017856A>T GRCh38
NC_000012.11:g.10170455A>T , CM000674.1:g.10170455A>T GRCh37
NC_000012.10:g.10061722A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338896.11:c.681-475A>T MANE Select ENSP00000344563.5:n.681-475A>T
ENST00000338896.10:c.681-475A>T ENSP00000344563.5:n.681-475A>T
ENST00000338896.9:c.681-475A>T ENSP00000344563.5:n.681-475A>T
ENST00000396502.5:c.*2110A>T ENSP00000379759.1:n.*2110A>T
ENST00000539155.1:c.*2603A>T ENSP00000444909.1:n.*2603A>T
ENST00000544853.5:c.*129-475A>T ENSP00000439561.1:n.*129-475A>T
NM_001129998.1:c.681-475A>T NP_001123470.1:n.681-475A>T
NM_205852.2:c.*2110A>T NP_995324.2:n.*2110A>T
NR_120484.1:n.249-2083T>A
XM_006719070.2:c.681-562A>T XP_006719133.1:n.681-562A>T
XM_006719071.2:c.*3-475A>T XP_006719134.1:n.*3-475A>T
XM_006719072.1:c.*883A>T XP_006719135.1:n.*883A>T
XM_011520658.1:c.654-475A>T XP_011518960.1:n.654-475A>T
XM_011520659.1:c.*859A>T XP_011518961.1:n.*859A>T
XM_011520660.1:c.*854A>T XP_011518962.1:n.*854A>T
XM_011520661.1:c.*10-475A>T XP_011518963.1:n.*10-475A>T
XM_011520662.1:c.*890A>T XP_011518964.1:n.*890A>T
XM_011520663.1:c.526-475A>T XP_011518965.1:n.526-475A>T
XM_011520664.1:c.526-562A>T XP_011518966.1:n.526-562A>T
XR_242889.3:n.956-475A>T
XR_931290.1:n.1836A>T
NM_001129998.2:c.681-475A>T NP_001123470.1:n.681-475A>T
NM_001319241.1:c.372-475A>T NP_001306170.1:n.372-475A>T
NM_001319242.1:c.*2110A>T NP_001306171.1:n.*2110A>T
NM_205852.3:c.*2110A>T NP_995324.2:n.*2110A>T
NR_135049.1:n.961-475A>T
XM_011520658.2:c.654-475A>T XP_011518960.1:n.654-475A>T
XM_011520663.2:c.526-475A>T XP_011518965.1:n.526-475A>T
XM_017019295.1:c.372-475A>T XP_016874784.1:n.372-475A>T
XM_024448976.1:c.681-562A>T XP_024304744.1:n.681-562A>T
XM_024448977.1:c.*2117A>T XP_024304745.1:n.*2117A>T
XR_002957401.1:n.106-1708T>A
NM_001129998.3:c.681-475A>T MANE Select NP_001123470.1:n.681-475A>T
NM_001387138.1:c.681-562A>T NP_001374067.1:n.681-562A>T
NR_169587.1:n.258-1708T>A