Canonical Allele Identifier: CA2725586788
Gene: CLEC12B HGNC NCBI

Linked Data

dbSNP Id: rs2137279596

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017726A>C , CM000674.2:g.10017726A>C GRCh38
NC_000012.11:g.10170325A>C , CM000674.1:g.10170325A>C GRCh37
NC_000012.10:g.10061592A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338896.11:c.681-605A>C MANE Select ENSP00000344563.5:n.681-605A>C
ENST00000338896.10:c.681-605A>C ENSP00000344563.5:n.681-605A>C
ENST00000338896.9:c.681-605A>C ENSP00000344563.5:n.681-605A>C
ENST00000396502.5:c.*1980A>C ENSP00000379759.1:n.*1980A>C
ENST00000539155.1:c.*2473A>C ENSP00000444909.1:n.*2473A>C
ENST00000544853.5:c.*129-605A>C ENSP00000439561.1:n.*129-605A>C
NM_001129998.1:c.681-605A>C NP_001123470.1:n.681-605A>C
NM_205852.2:c.*1980A>C NP_995324.2:n.*1980A>C
NR_120484.1:n.249-1953T>G
XM_006719070.2:c.681-692A>C XP_006719133.1:n.681-692A>C
XM_006719071.2:c.*3-605A>C XP_006719134.1:n.*3-605A>C
XM_006719072.1:c.*753A>C XP_006719135.1:n.*753A>C
XM_011520658.1:c.654-605A>C XP_011518960.1:n.654-605A>C
XM_011520659.1:c.*729A>C XP_011518961.1:n.*729A>C
XM_011520660.1:c.*724A>C XP_011518962.1:n.*724A>C
XM_011520661.1:c.*10-605A>C XP_011518963.1:n.*10-605A>C
XM_011520662.1:c.*760A>C XP_011518964.1:n.*760A>C
XM_011520663.1:c.526-605A>C XP_011518965.1:n.526-605A>C
XM_011520664.1:c.526-692A>C XP_011518966.1:n.526-692A>C
XR_242889.3:n.956-605A>C
XR_931290.1:n.1706A>C
NM_001129998.2:c.681-605A>C NP_001123470.1:n.681-605A>C
NM_001319241.1:c.372-605A>C NP_001306170.1:n.372-605A>C
NM_001319242.1:c.*1980A>C NP_001306171.1:n.*1980A>C
NM_205852.3:c.*1980A>C NP_995324.2:n.*1980A>C
NR_135049.1:n.961-605A>C
XM_011520658.2:c.654-605A>C XP_011518960.1:n.654-605A>C
XM_011520663.2:c.526-605A>C XP_011518965.1:n.526-605A>C
XM_017019295.1:c.372-605A>C XP_016874784.1:n.372-605A>C
XM_024448976.1:c.681-692A>C XP_024304744.1:n.681-692A>C
XM_024448977.1:c.*1987A>C XP_024304745.1:n.*1987A>C
XR_002957401.1:n.106-1578T>G
NM_001129998.3:c.681-605A>C MANE Select NP_001123470.1:n.681-605A>C
NM_001387138.1:c.681-692A>C NP_001374067.1:n.681-692A>C
NR_169587.1:n.258-1578T>G