Canonical Allele Identifier: CA944652602

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1865526900
• gnomAD v3: 12-10017884-C-A
• gnomAD v4: 12-10017884-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017884C>A , CM000674.2:g.10017884C>A	GRCh38
NC_000012.11:g.10170483C>A , CM000674.1:g.10170483C>A	GRCh37
NC_000012.10:g.10061750C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-447C>A MANE Select	ENSP00000344563.5:n.681-447C>A
ENST00000338896.10:c.681-447C>A	ENSP00000344563.5:n.681-447C>A
ENST00000338896.9:c.681-447C>A	ENSP00000344563.5:n.681-447C>A
ENST00000396502.5:c.*2138C>A	ENSP00000379759.1:n.*2138C>A
ENST00000539155.1:c.*2631C>A	ENSP00000444909.1:n.*2631C>A
ENST00000544853.5:c.*129-447C>A	ENSP00000439561.1:n.*129-447C>A
NM_001129998.1:c.681-447C>A	NP_001123470.1:n.681-447C>A
NM_205852.2:c.*2138C>A	NP_995324.2:n.*2138C>A
NR_120484.1:n.249-2111G>T
XM_006719070.2:c.681-534C>A	XP_006719133.1:n.681-534C>A
XM_006719071.2:c.*3-447C>A	XP_006719134.1:n.*3-447C>A
XM_006719072.1:c.*911C>A	XP_006719135.1:n.*911C>A
XM_011520658.1:c.654-447C>A	XP_011518960.1:n.654-447C>A
XM_011520659.1:c.*887C>A	XP_011518961.1:n.*887C>A
XM_011520660.1:c.*882C>A	XP_011518962.1:n.*882C>A
XM_011520661.1:c.*10-447C>A	XP_011518963.1:n.*10-447C>A
XM_011520662.1:c.*918C>A	XP_011518964.1:n.*918C>A
XM_011520663.1:c.526-447C>A	XP_011518965.1:n.526-447C>A
XM_011520664.1:c.526-534C>A	XP_011518966.1:n.526-534C>A
XR_242889.3:n.956-447C>A
XR_931290.1:n.1864C>A
NM_001129998.2:c.681-447C>A	NP_001123470.1:n.681-447C>A
NM_001319241.1:c.372-447C>A	NP_001306170.1:n.372-447C>A
NM_001319242.1:c.*2138C>A	NP_001306171.1:n.*2138C>A
NM_205852.3:c.*2138C>A	NP_995324.2:n.*2138C>A
NR_135049.1:n.961-447C>A
XM_011520658.2:c.654-447C>A	XP_011518960.1:n.654-447C>A
XM_011520663.2:c.526-447C>A	XP_011518965.1:n.526-447C>A
XM_017019295.1:c.372-447C>A	XP_016874784.1:n.372-447C>A
XM_024448976.1:c.681-534C>A	XP_024304744.1:n.681-534C>A
XM_024448977.1:c.*2145C>A	XP_024304745.1:n.*2145C>A
XR_002957401.1:n.106-1736G>T
NM_001129998.3:c.681-447C>A MANE Select	NP_001123470.1:n.681-447C>A
NM_001387138.1:c.681-534C>A	NP_001374067.1:n.681-534C>A
NR_169587.1:n.258-1736G>T