Canonical Allele Identifier: CA232780245

Gene: CLEC12B

Linked Data

• dbSNP Id: rs993775488
• gnomAD v3: 12-10017605-T-C
• gnomAD v4: 12-10017605-T-C
• MyVariant Identifiers: chr12:g.10170204T>C (hg19) ; chr12:g.10017605T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017605T>C , CM000674.2:g.10017605T>C	GRCh38
NC_000012.11:g.10170204T>C , CM000674.1:g.10170204T>C	GRCh37
NC_000012.10:g.10061471T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-726T>C MANE Select	ENSP00000344563.5:n.681-726T>C
ENST00000338896.10:c.681-726T>C	ENSP00000344563.5:n.681-726T>C
ENST00000338896.9:c.681-726T>C	ENSP00000344563.5:n.681-726T>C
ENST00000396502.5:c.*1859T>C	ENSP00000379759.1:n.*1859T>C
ENST00000539155.1:c.*2352T>C	ENSP00000444909.1:n.*2352T>C
ENST00000544853.5:c.*129-726T>C	ENSP00000439561.1:n.*129-726T>C
NM_001129998.1:c.681-726T>C	NP_001123470.1:n.681-726T>C
NM_205852.2:c.*1859T>C	NP_995324.2:n.*1859T>C
NR_120484.1:n.249-1832A>G
XM_006719070.2:c.681-813T>C	XP_006719133.1:n.681-813T>C
XM_006719071.2:c.*3-726T>C	XP_006719134.1:n.*3-726T>C
XM_006719072.1:c.*632T>C	XP_006719135.1:n.*632T>C
XM_011520658.1:c.654-726T>C	XP_011518960.1:n.654-726T>C
XM_011520659.1:c.*608T>C	XP_011518961.1:n.*608T>C
XM_011520660.1:c.*603T>C	XP_011518962.1:n.*603T>C
XM_011520661.1:c.*10-726T>C	XP_011518963.1:n.*10-726T>C
XM_011520662.1:c.*639T>C	XP_011518964.1:n.*639T>C
XM_011520663.1:c.526-726T>C	XP_011518965.1:n.526-726T>C
XM_011520664.1:c.526-813T>C	XP_011518966.1:n.526-813T>C
XR_242889.3:n.956-726T>C
XR_931290.1:n.1585T>C
NM_001129998.2:c.681-726T>C	NP_001123470.1:n.681-726T>C
NM_001319241.1:c.372-726T>C	NP_001306170.1:n.372-726T>C
NM_001319242.1:c.*1859T>C	NP_001306171.1:n.*1859T>C
NM_205852.3:c.*1859T>C	NP_995324.2:n.*1859T>C
NR_135049.1:n.961-726T>C
XM_011520658.2:c.654-726T>C	XP_011518960.1:n.654-726T>C
XM_011520663.2:c.526-726T>C	XP_011518965.1:n.526-726T>C
XM_017019295.1:c.372-726T>C	XP_016874784.1:n.372-726T>C
XM_024448976.1:c.681-813T>C	XP_024304744.1:n.681-813T>C
XM_024448977.1:c.*1866T>C	XP_024304745.1:n.*1866T>C
XR_002957401.1:n.106-1457A>G
NM_001129998.3:c.681-726T>C MANE Select	NP_001123470.1:n.681-726T>C
NM_001387138.1:c.681-813T>C	NP_001374067.1:n.681-813T>C
NR_169587.1:n.258-1457A>G