Canonical Allele Identifier: CA2015750835

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1865529590
• gnomAD v4: 12-10018017-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10018017G>A , CM000674.2:g.10018017G>A	GRCh38
NC_000012.11:g.10170616G>A , CM000674.1:g.10170616G>A	GRCh37
NC_000012.10:g.10061883G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-314G>A MANE Select	ENSP00000344563.5:n.681-314G>A
ENST00000338896.10:c.681-314G>A	ENSP00000344563.5:n.681-314G>A
ENST00000338896.9:c.681-314G>A	ENSP00000344563.5:n.681-314G>A
ENST00000544853.5:c.*129-314G>A	ENSP00000439561.1:n.*129-314G>A
NM_001129998.1:c.681-314G>A	NP_001123470.1:n.681-314G>A
NR_120484.1:n.249-2244C>T
XM_006719070.2:c.681-401G>A	XP_006719133.1:n.681-401G>A
XM_006719071.2:c.*3-314G>A	XP_006719134.1:n.*3-314G>A
XM_011520658.1:c.654-314G>A	XP_011518960.1:n.654-314G>A
XM_011520661.1:c.*10-314G>A	XP_011518963.1:n.*10-314G>A
XM_011520663.1:c.526-314G>A	XP_011518965.1:n.526-314G>A
XM_011520664.1:c.526-401G>A	XP_011518966.1:n.526-401G>A
XR_242889.3:n.956-314G>A
NM_001129998.2:c.681-314G>A	NP_001123470.1:n.681-314G>A
NM_001319241.1:c.372-314G>A	NP_001306170.1:n.372-314G>A
NR_135049.1:n.961-314G>A
XM_011520658.2:c.654-314G>A	XP_011518960.1:n.654-314G>A
XM_011520663.2:c.526-314G>A	XP_011518965.1:n.526-314G>A
XM_017019295.1:c.372-314G>A	XP_016874784.1:n.372-314G>A
XM_024448976.1:c.681-401G>A	XP_024304744.1:n.681-401G>A
XR_002957401.1:n.106-1869C>T
NM_001129998.3:c.681-314G>A MANE Select	NP_001123470.1:n.681-314G>A
NM_001387138.1:c.681-401G>A	NP_001374067.1:n.681-401G>A
NR_169587.1:n.258-1869C>T