Canonical Allele Identifier: CA1910259531

Gene: MBL2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52771902T= , CM000672.2:g.52771902T=	GRCh38
NC_000010.10:g.54531662T= , CM000672.1:g.54531662T=	GRCh37
NC_000010.9:g.54201668T=	NCBI36
NG_008196.1:g.4799A= , LRG_154:g.4799A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674931.1:c.-9-258A= MANE Select	ENSP00000502789.1:n.-9-258A=
ENST00000675947.1:c.-24-243A=	ENSP00000502615.1:n.-24-243A=
XM_006717861.2:c.-24-243A=	XP_006717924.1:n.-24-243A=
XM_011539816.1:c.-9-258A=	XP_011538118.1:n.-9-258A=
XM_006717861.4:c.-24-243A=	XP_006717924.1:n.-24-243A=
XM_011539816.3:c.-9-258A=	XP_011538118.1:n.-9-258A=
NM_001378373.1:c.-9-258A= MANE Select	NP_001365302.1:n.-9-258A=
NM_001378374.1:c.-24-243A=	NP_001365303.1:n.-24-243A=