Canonical Allele Identifier: CA232780221

Gene: CLEC12B

Linked Data

• dbSNP Id: rs151006399
• gnomAD v2: 12-10170162-C-G
• gnomAD v3: 12-10017563-C-G
• gnomAD v4: 12-10017563-C-G
• MyVariant Identifiers: chr12:g.10170162C>G (hg19) ; chr12:g.10017563C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017563C>G , CM000674.2:g.10017563C>G	GRCh38
NC_000012.11:g.10170162C>G , CM000674.1:g.10170162C>G	GRCh37
NC_000012.10:g.10061429C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-768C>G MANE Select	ENSP00000344563.5:n.681-768C>G
ENST00000338896.10:c.681-768C>G	ENSP00000344563.5:n.681-768C>G
ENST00000338896.9:c.681-768C>G	ENSP00000344563.5:n.681-768C>G
ENST00000396502.5:c.*1817C>G	ENSP00000379759.1:n.*1817C>G
ENST00000539155.1:c.*2310C>G	ENSP00000444909.1:n.*2310C>G
ENST00000544853.5:c.*129-768C>G	ENSP00000439561.1:n.*129-768C>G
NM_001129998.1:c.681-768C>G	NP_001123470.1:n.681-768C>G
NM_205852.2:c.*1817C>G	NP_995324.2:n.*1817C>G
NR_120484.1:n.249-1790G>C
XM_006719070.2:c.681-855C>G	XP_006719133.1:n.681-855C>G
XM_006719071.2:c.*3-768C>G	XP_006719134.1:n.*3-768C>G
XM_006719072.1:c.*590C>G	XP_006719135.1:n.*590C>G
XM_011520658.1:c.654-768C>G	XP_011518960.1:n.654-768C>G
XM_011520659.1:c.*566C>G	XP_011518961.1:n.*566C>G
XM_011520660.1:c.*561C>G	XP_011518962.1:n.*561C>G
XM_011520661.1:c.*10-768C>G	XP_011518963.1:n.*10-768C>G
XM_011520662.1:c.*597C>G	XP_011518964.1:n.*597C>G
XM_011520663.1:c.526-768C>G	XP_011518965.1:n.526-768C>G
XM_011520664.1:c.526-855C>G	XP_011518966.1:n.526-855C>G
XR_242889.3:n.956-768C>G
XR_931290.1:n.1543C>G
NM_001129998.2:c.681-768C>G	NP_001123470.1:n.681-768C>G
NM_001319241.1:c.372-768C>G	NP_001306170.1:n.372-768C>G
NM_001319242.1:c.*1817C>G	NP_001306171.1:n.*1817C>G
NM_205852.3:c.*1817C>G	NP_995324.2:n.*1817C>G
NR_135049.1:n.961-768C>G
XM_011520658.2:c.654-768C>G	XP_011518960.1:n.654-768C>G
XM_011520663.2:c.526-768C>G	XP_011518965.1:n.526-768C>G
XM_017019295.1:c.372-768C>G	XP_016874784.1:n.372-768C>G
XM_024448976.1:c.681-855C>G	XP_024304744.1:n.681-855C>G
XM_024448977.1:c.*1824C>G	XP_024304745.1:n.*1824C>G
XR_002957401.1:n.106-1415G>C
NM_001129998.3:c.681-768C>G MANE Select	NP_001123470.1:n.681-768C>G
NM_001387138.1:c.681-855C>G	NP_001374067.1:n.681-855C>G
NR_169587.1:n.258-1415G>C