Canonical Allele Identifier: CA1910259429

Gene: MBL2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52771682T= , CM000672.2:g.52771682T=	GRCh38
NC_000010.10:g.54531442T= , CM000672.1:g.54531442T=	GRCh37
NC_000010.9:g.54201448T=	NCBI36
NG_008196.1:g.5019A= , LRG_154:g.5019A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000674931.1:c.-9-38A= MANE Select	ENSP00000502789.1:n.-9-38A=
ENST00000675947.1:c.-24-23A=	ENSP00000502615.1:n.-24-23A=
ENST00000373968.3:c.-47A=	ENSP00000363079.3:n.-47A=
NM_000242.2:c.-47A= , LRG_154t1:c.-47A=	NP_000233.1:n.-47A=
XM_006717861.2:c.-24-23A=	XP_006717924.1:n.-24-23A=
XM_011539816.1:c.-9-38A=	XP_011538118.1:n.-9-38A=
XM_006717861.4:c.-24-23A=	XP_006717924.1:n.-24-23A=
XM_011539816.3:c.-9-38A=	XP_011538118.1:n.-9-38A=
NM_001378373.1:c.-9-38A= MANE Select	NP_001365302.1:n.-9-38A=
NM_001378374.1:c.-24-23A=	NP_001365303.1:n.-24-23A=