Canonical Allele Identifier: CA2323507855

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665742C= , CM000681.2:g.12665742C=	GRCh38
NC_000019.9:g.12776556C= , CM000681.1:g.12776556C=	GRCh37
NC_000019.8:g.12637556C=	NCBI36
NG_008318.1:g.6036G=
NG_015814.1:g.3939C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.223G= MANE Select	ENSP00000395473.2:p.Val75=
ENST00000221363.8:c.223G=	ENSP00000221363.4:p.Val75=
ENST00000456935.6:c.223G=	ENSP00000395473.2:p.Val75=
ENST00000466794.5:n.205G=
ENST00000486847.2:c.160-217G=	ENSP00000470174.1:n.160-217G=
ENST00000596512.5:n.201-217G=
ENST00000597961.1:c.214G=	ENSP00000472710.1:p.Val72=
ENST00000598876.1:c.250G=	ENSP00000470533.1:p.Val84=
ENST00000600281.1:n.264G=
NM_000528.3:c.223G=	NP_000519.2:p.Val75=
NM_001173498.1:c.223G=	NP_001166969.1:p.Val75=
XM_005259913.1:c.223G=	XP_005259970.1:p.Val75=
XM_005259913.2:c.223G=	XP_005259970.1:p.Val75=
XM_024451518.1:c.-796G=	XP_024307286.1:n.-796G=
NM_000528.4:c.223G= MANE Select	NP_000519.2:p.Val75=
NM_001173498.2:c.223G=	NP_001166969.1:p.Val75=