Canonical Allele Identifier: CA682609224

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1420996972
• gnomAD v3: 12-10017701-T-C
• gnomAD v4: 12-10017701-T-C
• MyVariant Identifiers: chr12:g.10170300T>C (hg19) ; chr12:g.10017701T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017701T>C , CM000674.2:g.10017701T>C	GRCh38
NC_000012.11:g.10170300T>C , CM000674.1:g.10170300T>C	GRCh37
NC_000012.10:g.10061567T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-630T>C MANE Select	ENSP00000344563.5:n.681-630T>C
ENST00000338896.10:c.681-630T>C	ENSP00000344563.5:n.681-630T>C
ENST00000338896.9:c.681-630T>C	ENSP00000344563.5:n.681-630T>C
ENST00000396502.5:c.*1955T>C	ENSP00000379759.1:n.*1955T>C
ENST00000539155.1:c.*2448T>C	ENSP00000444909.1:n.*2448T>C
ENST00000544853.5:c.*129-630T>C	ENSP00000439561.1:n.*129-630T>C
NM_001129998.1:c.681-630T>C	NP_001123470.1:n.681-630T>C
NM_205852.2:c.*1955T>C	NP_995324.2:n.*1955T>C
NR_120484.1:n.249-1928A>G
XM_006719070.2:c.681-717T>C	XP_006719133.1:n.681-717T>C
XM_006719071.2:c.*3-630T>C	XP_006719134.1:n.*3-630T>C
XM_006719072.1:c.*728T>C	XP_006719135.1:n.*728T>C
XM_011520658.1:c.654-630T>C	XP_011518960.1:n.654-630T>C
XM_011520659.1:c.*704T>C	XP_011518961.1:n.*704T>C
XM_011520660.1:c.*699T>C	XP_011518962.1:n.*699T>C
XM_011520661.1:c.*10-630T>C	XP_011518963.1:n.*10-630T>C
XM_011520662.1:c.*735T>C	XP_011518964.1:n.*735T>C
XM_011520663.1:c.526-630T>C	XP_011518965.1:n.526-630T>C
XM_011520664.1:c.526-717T>C	XP_011518966.1:n.526-717T>C
XR_242889.3:n.956-630T>C
XR_931290.1:n.1681T>C
NM_001129998.2:c.681-630T>C	NP_001123470.1:n.681-630T>C
NM_001319241.1:c.372-630T>C	NP_001306170.1:n.372-630T>C
NM_001319242.1:c.*1955T>C	NP_001306171.1:n.*1955T>C
NM_205852.3:c.*1955T>C	NP_995324.2:n.*1955T>C
NR_135049.1:n.961-630T>C
XM_011520658.2:c.654-630T>C	XP_011518960.1:n.654-630T>C
XM_011520663.2:c.526-630T>C	XP_011518965.1:n.526-630T>C
XM_017019295.1:c.372-630T>C	XP_016874784.1:n.372-630T>C
XM_024448976.1:c.681-717T>C	XP_024304744.1:n.681-717T>C
XM_024448977.1:c.*1962T>C	XP_024304745.1:n.*1962T>C
XR_002957401.1:n.106-1553A>G
NM_001129998.3:c.681-630T>C MANE Select	NP_001123470.1:n.681-630T>C
NM_001387138.1:c.681-717T>C	NP_001374067.1:n.681-717T>C
NR_169587.1:n.258-1553A>G