Canonical Allele Identifier: CA232771480

Gene: CLEC12B CLEC1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10012878T>C , CM000674.2:g.10012878T>C	GRCh38
NC_000012.11:g.10165477T>C , CM000674.1:g.10165477T>C	GRCh37
NC_000012.10:g.10056744T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001129998.3:c.185T>C (CLEC12B) MANE Select	NP_001123470.1:p.Met62Thr
ENST00000338896.11:c.185T>C (CLEC12B) MANE Select	ENSP00000344563.5:p.Met62Thr
NM_001129998.1:c.185T>C (CLEC12B)	NP_001123470.1:p.Met62Thr
NM_001129998.2:c.185T>C (CLEC12B)	NP_001123470.1:p.Met62Thr
NM_001319241.1:c.-117T>C (CLEC12B)	NP_001306170.1:n.-117T>C
NM_001319242.1:c.-117T>C (CLEC12B)	NP_001306171.1:n.-117T>C
NM_001387138.1:c.185T>C (CLEC12B)	NP_001374067.1:p.Met62Thr
NM_205852.2:c.185T>C (CLEC12B)	NP_995324.2:p.Met62Thr
NM_205852.3:c.185T>C (CLEC12B)	NP_995324.2:p.Met62Thr
NR_135049.1:n.318T>C (CLEC12B)
ENST00000338896.10:c.185T>C (CLEC12B)	ENSP00000344563.5:p.Met62Thr
ENST00000338896.9:c.185T>C (CLEC12B)	ENSP00000344563.5:p.Met62Thr
ENST00000396502.5:c.185T>C (CLEC12B)	ENSP00000379759.1:p.Met62Thr
ENST00000428126.6:c.-247+523A>G (CLEC1B)	ENSP00000406338.2:n.-247+523A>G
ENST00000535903.1:n.186T>C (CLEC12B)
ENST00000539155.1:c.185T>C (CLEC12B)	ENSP00000444909.1:p.Met62Thr
ENST00000544853.5:c.185T>C (CLEC12B)	ENSP00000439561.1:p.Met62Thr
XM_006719070.2:c.185T>C (CLEC12B)	XP_006719133.1:p.Met62Thr
XM_006719071.2:c.185T>C (CLEC12B)	XP_006719134.1:p.Met62Thr
XM_006719072.1:c.185T>C (CLEC12B)	XP_006719135.1:p.Met62Thr
XM_011520658.1:c.158T>C (CLEC12B)	XP_011518960.1:p.Met53Thr
XM_011520658.2:c.158T>C (CLEC12B)	XP_011518960.1:p.Met53Thr
XM_011520659.1:c.185T>C (CLEC12B)	XP_011518961.1:p.Met62Thr
XM_011520660.1:c.185T>C (CLEC12B)	XP_011518962.1:p.Met62Thr
XM_011520661.1:c.185T>C (CLEC12B)	XP_011518963.1:p.Met62Thr
XM_011520662.1:c.185T>C (CLEC12B)	XP_011518964.1:p.Met62Thr
XM_011520663.1:c.185T>C (CLEC12B)	XP_011518965.1:p.Met62Thr
XM_011520663.2:c.185T>C (CLEC12B)	XP_011518965.1:p.Met62Thr
XM_011520664.1:c.185T>C (CLEC12B)	XP_011518966.1:p.Met62Thr
XM_017019295.1:c.-117T>C (CLEC12B)	XP_016874784.1:n.-117T>C
XM_024448976.1:c.185T>C (CLEC12B)	XP_024304744.1:p.Met62Thr
XM_024448977.1:c.185T>C (CLEC12B)	XP_024304745.1:p.Met62Thr
XR_242889.3:n.313T>C (CLEC12B)
XR_931290.1:n.313T>C (CLEC12B)