Canonical Allele Identifier: CA2015750611

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1865514719

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017462C>G , CM000674.2:g.10017462C>G	GRCh38
NC_000012.11:g.10170061C>G , CM000674.1:g.10170061C>G	GRCh37
NC_000012.10:g.10061328C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338896.11:c.681-869C>G MANE Select	ENSP00000344563.5:n.681-869C>G
ENST00000338896.10:c.681-869C>G	ENSP00000344563.5:n.681-869C>G
ENST00000338896.9:c.681-869C>G	ENSP00000344563.5:n.681-869C>G
ENST00000396502.5:c.*1716C>G	ENSP00000379759.1:n.*1716C>G
ENST00000539155.1:c.*2209C>G	ENSP00000444909.1:n.*2209C>G
ENST00000544853.5:c.*129-869C>G	ENSP00000439561.1:n.*129-869C>G
NM_001129998.1:c.681-869C>G	NP_001123470.1:n.681-869C>G
NM_205852.2:c.*1716C>G	NP_995324.2:n.*1716C>G
NR_120484.1:n.249-1689G>C
XM_006719070.2:c.681-956C>G	XP_006719133.1:n.681-956C>G
XM_006719071.2:c.*3-869C>G	XP_006719134.1:n.*3-869C>G
XM_006719072.1:c.*489C>G	XP_006719135.1:n.*489C>G
XM_011520658.1:c.654-869C>G	XP_011518960.1:n.654-869C>G
XM_011520659.1:c.*465C>G	XP_011518961.1:n.*465C>G
XM_011520660.1:c.*460C>G	XP_011518962.1:n.*460C>G
XM_011520661.1:c.*10-869C>G	XP_011518963.1:n.*10-869C>G
XM_011520662.1:c.*496C>G	XP_011518964.1:n.*496C>G
XM_011520663.1:c.526-869C>G	XP_011518965.1:n.526-869C>G
XM_011520664.1:c.526-956C>G	XP_011518966.1:n.526-956C>G
XR_242889.3:n.956-869C>G
XR_931290.1:n.1442C>G
NM_001129998.2:c.681-869C>G	NP_001123470.1:n.681-869C>G
NM_001319241.1:c.372-869C>G	NP_001306170.1:n.372-869C>G
NM_001319242.1:c.*1716C>G	NP_001306171.1:n.*1716C>G
NM_205852.3:c.*1716C>G	NP_995324.2:n.*1716C>G
NR_135049.1:n.961-869C>G
XM_011520658.2:c.654-869C>G	XP_011518960.1:n.654-869C>G
XM_011520663.2:c.526-869C>G	XP_011518965.1:n.526-869C>G
XM_017019295.1:c.372-869C>G	XP_016874784.1:n.372-869C>G
XM_024448976.1:c.681-956C>G	XP_024304744.1:n.681-956C>G
XM_024448977.1:c.*1723C>G	XP_024304745.1:n.*1723C>G
XR_002957401.1:n.106-1314G>C
NM_001129998.3:c.681-869C>G MANE Select	NP_001123470.1:n.681-869C>G
NM_001387138.1:c.681-956C>G	NP_001374067.1:n.681-956C>G
NR_169587.1:n.258-1314G>C