Canonical Allele Identifier: CA2015750622
Gene: CLEC12B HGNC NCBI

Linked Data

dbSNP Id: rs1415193574

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017495G>A , CM000674.2:g.10017495G>A GRCh38
NC_000012.11:g.10170094G>A , CM000674.1:g.10170094G>A GRCh37
NC_000012.10:g.10061361G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000338896.11:c.681-836G>A MANE Select ENSP00000344563.5:n.681-836G>A
ENST00000338896.10:c.681-836G>A ENSP00000344563.5:n.681-836G>A
ENST00000338896.9:c.681-836G>A ENSP00000344563.5:n.681-836G>A
ENST00000396502.5:c.*1749G>A ENSP00000379759.1:n.*1749G>A
ENST00000539155.1:c.*2242G>A ENSP00000444909.1:n.*2242G>A
ENST00000544853.5:c.*129-836G>A ENSP00000439561.1:n.*129-836G>A
NM_001129998.1:c.681-836G>A NP_001123470.1:n.681-836G>A
NM_205852.2:c.*1749G>A NP_995324.2:n.*1749G>A
NR_120484.1:n.249-1722C>T
XM_006719070.2:c.681-923G>A XP_006719133.1:n.681-923G>A
XM_006719071.2:c.*3-836G>A XP_006719134.1:n.*3-836G>A
XM_006719072.1:c.*522G>A XP_006719135.1:n.*522G>A
XM_011520658.1:c.654-836G>A XP_011518960.1:n.654-836G>A
XM_011520659.1:c.*498G>A XP_011518961.1:n.*498G>A
XM_011520660.1:c.*493G>A XP_011518962.1:n.*493G>A
XM_011520661.1:c.*10-836G>A XP_011518963.1:n.*10-836G>A
XM_011520662.1:c.*529G>A XP_011518964.1:n.*529G>A
XM_011520663.1:c.526-836G>A XP_011518965.1:n.526-836G>A
XM_011520664.1:c.526-923G>A XP_011518966.1:n.526-923G>A
XR_242889.3:n.956-836G>A
XR_931290.1:n.1475G>A
NM_001129998.2:c.681-836G>A NP_001123470.1:n.681-836G>A
NM_001319241.1:c.372-836G>A NP_001306170.1:n.372-836G>A
NM_001319242.1:c.*1749G>A NP_001306171.1:n.*1749G>A
NM_205852.3:c.*1749G>A NP_995324.2:n.*1749G>A
NR_135049.1:n.961-836G>A
XM_011520658.2:c.654-836G>A XP_011518960.1:n.654-836G>A
XM_011520663.2:c.526-836G>A XP_011518965.1:n.526-836G>A
XM_017019295.1:c.372-836G>A XP_016874784.1:n.372-836G>A
XM_024448976.1:c.681-923G>A XP_024304744.1:n.681-923G>A
XM_024448977.1:c.*1756G>A XP_024304745.1:n.*1756G>A
XR_002957401.1:n.106-1347C>T
NM_001129998.3:c.681-836G>A MANE Select NP_001123470.1:n.681-836G>A
NM_001387138.1:c.681-923G>A NP_001374067.1:n.681-923G>A
NR_169587.1:n.258-1347C>T