Canonical Allele Identifier: CA2323499558

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649156C= , CM000681.2:g.12649156C=	GRCh38
NC_000019.9:g.12759970C= , CM000681.1:g.12759970C=	GRCh37
NC_000019.8:g.12620970C=	NCBI36
NG_008318.1:g.22622G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2416G= MANE Select	ENSP00000395473.2:p.Asp806=
ENST00000221363.8:c.2413G=	ENSP00000221363.4:p.Asp805=
ENST00000456935.6:c.2416G=	ENSP00000395473.2:p.Asp806=
ENST00000466794.5:n.3006G=
NM_000528.3:c.2416G=	NP_000519.2:p.Asp806=
NM_001173498.1:c.2413G=	NP_001166969.1:p.Asp805=
XM_005259913.1:c.2419G=	XP_005259970.1:p.Asp807=
XM_011528017.1:c.1315G=	XP_011526319.1:p.Asp439=
XM_005259913.2:c.2419G=	XP_005259970.1:p.Asp807=
XM_024451518.1:c.1315G=	XP_024307286.1:p.Asp439=
NM_000528.4:c.2416G= MANE Select	NP_000519.2:p.Asp806=
NM_001173498.2:c.2413G=	NP_001166969.1:p.Asp805=