Canonical Allele Identifier: CA682609186

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1488693169
• gnomAD v4: 12-10017624-T-C
• MyVariant Identifiers: chr12:g.10170223T>C (hg19) ; chr12:g.10017624T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017624T>C , CM000674.2:g.10017624T>C	GRCh38
NC_000012.11:g.10170223T>C , CM000674.1:g.10170223T>C	GRCh37
NC_000012.10:g.10061490T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338896.11:c.681-707T>C MANE Select	ENSP00000344563.5:n.681-707T>C
ENST00000338896.10:c.681-707T>C	ENSP00000344563.5:n.681-707T>C
ENST00000338896.9:c.681-707T>C	ENSP00000344563.5:n.681-707T>C
ENST00000396502.5:c.*1878T>C	ENSP00000379759.1:n.*1878T>C
ENST00000539155.1:c.*2371T>C	ENSP00000444909.1:n.*2371T>C
ENST00000544853.5:c.*129-707T>C	ENSP00000439561.1:n.*129-707T>C
NM_001129998.1:c.681-707T>C	NP_001123470.1:n.681-707T>C
NM_205852.2:c.*1878T>C	NP_995324.2:n.*1878T>C
NR_120484.1:n.249-1851A>G
XM_006719070.2:c.681-794T>C	XP_006719133.1:n.681-794T>C
XM_006719071.2:c.*3-707T>C	XP_006719134.1:n.*3-707T>C
XM_006719072.1:c.*651T>C	XP_006719135.1:n.*651T>C
XM_011520658.1:c.654-707T>C	XP_011518960.1:n.654-707T>C
XM_011520659.1:c.*627T>C	XP_011518961.1:n.*627T>C
XM_011520660.1:c.*622T>C	XP_011518962.1:n.*622T>C
XM_011520661.1:c.*10-707T>C	XP_011518963.1:n.*10-707T>C
XM_011520662.1:c.*658T>C	XP_011518964.1:n.*658T>C
XM_011520663.1:c.526-707T>C	XP_011518965.1:n.526-707T>C
XM_011520664.1:c.526-794T>C	XP_011518966.1:n.526-794T>C
XR_242889.3:n.956-707T>C
XR_931290.1:n.1604T>C
NM_001129998.2:c.681-707T>C	NP_001123470.1:n.681-707T>C
NM_001319241.1:c.372-707T>C	NP_001306170.1:n.372-707T>C
NM_001319242.1:c.*1878T>C	NP_001306171.1:n.*1878T>C
NM_205852.3:c.*1878T>C	NP_995324.2:n.*1878T>C
NR_135049.1:n.961-707T>C
XM_011520658.2:c.654-707T>C	XP_011518960.1:n.654-707T>C
XM_011520663.2:c.526-707T>C	XP_011518965.1:n.526-707T>C
XM_017019295.1:c.372-707T>C	XP_016874784.1:n.372-707T>C
XM_024448976.1:c.681-794T>C	XP_024304744.1:n.681-794T>C
XM_024448977.1:c.*1885T>C	XP_024304745.1:n.*1885T>C
XR_002957401.1:n.106-1476A>G
NM_001129998.3:c.681-707T>C MANE Select	NP_001123470.1:n.681-707T>C
NM_001387138.1:c.681-794T>C	NP_001374067.1:n.681-794T>C
NR_169587.1:n.258-1476A>G