Canonical Allele Identifier: CA2617597636

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10017623-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017623C>T , CM000674.2:g.10017623C>T	GRCh38
NC_000012.11:g.10170222C>T , CM000674.1:g.10170222C>T	GRCh37
NC_000012.10:g.10061489C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-708C>T MANE Select	ENSP00000344563.5:n.681-708C>T
ENST00000338896.10:c.681-708C>T	ENSP00000344563.5:n.681-708C>T
ENST00000338896.9:c.681-708C>T	ENSP00000344563.5:n.681-708C>T
ENST00000396502.5:c.*1877C>T	ENSP00000379759.1:n.*1877C>T
ENST00000539155.1:c.*2370C>T	ENSP00000444909.1:n.*2370C>T
ENST00000544853.5:c.*129-708C>T	ENSP00000439561.1:n.*129-708C>T
NM_001129998.1:c.681-708C>T	NP_001123470.1:n.681-708C>T
NM_205852.2:c.*1877C>T	NP_995324.2:n.*1877C>T
NR_120484.1:n.249-1850G>A
XM_006719070.2:c.681-795C>T	XP_006719133.1:n.681-795C>T
XM_006719071.2:c.*3-708C>T	XP_006719134.1:n.*3-708C>T
XM_006719072.1:c.*650C>T	XP_006719135.1:n.*650C>T
XM_011520658.1:c.654-708C>T	XP_011518960.1:n.654-708C>T
XM_011520659.1:c.*626C>T	XP_011518961.1:n.*626C>T
XM_011520660.1:c.*621C>T	XP_011518962.1:n.*621C>T
XM_011520661.1:c.*10-708C>T	XP_011518963.1:n.*10-708C>T
XM_011520662.1:c.*657C>T	XP_011518964.1:n.*657C>T
XM_011520663.1:c.526-708C>T	XP_011518965.1:n.526-708C>T
XM_011520664.1:c.526-795C>T	XP_011518966.1:n.526-795C>T
XR_242889.3:n.956-708C>T
XR_931290.1:n.1603C>T
NM_001129998.2:c.681-708C>T	NP_001123470.1:n.681-708C>T
NM_001319241.1:c.372-708C>T	NP_001306170.1:n.372-708C>T
NM_001319242.1:c.*1877C>T	NP_001306171.1:n.*1877C>T
NM_205852.3:c.*1877C>T	NP_995324.2:n.*1877C>T
NR_135049.1:n.961-708C>T
XM_011520658.2:c.654-708C>T	XP_011518960.1:n.654-708C>T
XM_011520663.2:c.526-708C>T	XP_011518965.1:n.526-708C>T
XM_017019295.1:c.372-708C>T	XP_016874784.1:n.372-708C>T
XM_024448976.1:c.681-795C>T	XP_024304744.1:n.681-795C>T
XM_024448977.1:c.*1884C>T	XP_024304745.1:n.*1884C>T
XR_002957401.1:n.106-1475G>A
NM_001129998.3:c.681-708C>T MANE Select	NP_001123470.1:n.681-708C>T
NM_001387138.1:c.681-795C>T	NP_001374067.1:n.681-795C>T
NR_169587.1:n.258-1475G>A