Canonical Allele Identifier: CA232780212

Gene: CLEC12B

Linked Data

• dbSNP Id: rs905615333
• gnomAD v4: 12-10017560-C-A
• MyVariant Identifiers: chr12:g.10170159C>A (hg19) ; chr12:g.10017560C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017560C>A , CM000674.2:g.10017560C>A	GRCh38
NC_000012.11:g.10170159C>A , CM000674.1:g.10170159C>A	GRCh37
NC_000012.10:g.10061426C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-771C>A MANE Select	ENSP00000344563.5:n.681-771C>A
ENST00000338896.10:c.681-771C>A	ENSP00000344563.5:n.681-771C>A
ENST00000338896.9:c.681-771C>A	ENSP00000344563.5:n.681-771C>A
ENST00000396502.5:c.*1814C>A	ENSP00000379759.1:n.*1814C>A
ENST00000539155.1:c.*2307C>A	ENSP00000444909.1:n.*2307C>A
ENST00000544853.5:c.*129-771C>A	ENSP00000439561.1:n.*129-771C>A
NM_001129998.1:c.681-771C>A	NP_001123470.1:n.681-771C>A
NM_205852.2:c.*1814C>A	NP_995324.2:n.*1814C>A
NR_120484.1:n.249-1787G>T
XM_006719070.2:c.681-858C>A	XP_006719133.1:n.681-858C>A
XM_006719071.2:c.*3-771C>A	XP_006719134.1:n.*3-771C>A
XM_006719072.1:c.*587C>A	XP_006719135.1:n.*587C>A
XM_011520658.1:c.654-771C>A	XP_011518960.1:n.654-771C>A
XM_011520659.1:c.*563C>A	XP_011518961.1:n.*563C>A
XM_011520660.1:c.*558C>A	XP_011518962.1:n.*558C>A
XM_011520661.1:c.*10-771C>A	XP_011518963.1:n.*10-771C>A
XM_011520662.1:c.*594C>A	XP_011518964.1:n.*594C>A
XM_011520663.1:c.526-771C>A	XP_011518965.1:n.526-771C>A
XM_011520664.1:c.526-858C>A	XP_011518966.1:n.526-858C>A
XR_242889.3:n.956-771C>A
XR_931290.1:n.1540C>A
NM_001129998.2:c.681-771C>A	NP_001123470.1:n.681-771C>A
NM_001319241.1:c.372-771C>A	NP_001306170.1:n.372-771C>A
NM_001319242.1:c.*1814C>A	NP_001306171.1:n.*1814C>A
NM_205852.3:c.*1814C>A	NP_995324.2:n.*1814C>A
NR_135049.1:n.961-771C>A
XM_011520658.2:c.654-771C>A	XP_011518960.1:n.654-771C>A
XM_011520663.2:c.526-771C>A	XP_011518965.1:n.526-771C>A
XM_017019295.1:c.372-771C>A	XP_016874784.1:n.372-771C>A
XM_024448976.1:c.681-858C>A	XP_024304744.1:n.681-858C>A
XM_024448977.1:c.*1821C>A	XP_024304745.1:n.*1821C>A
XR_002957401.1:n.106-1412G>T
NM_001129998.3:c.681-771C>A MANE Select	NP_001123470.1:n.681-771C>A
NM_001387138.1:c.681-858C>A	NP_001374067.1:n.681-858C>A
NR_169587.1:n.258-1412G>T