Canonical Allele Identifier: CA2323498716

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647594G= , CM000681.2:g.12647594G=	GRCh38
NC_000019.9:g.12758408G= , CM000681.1:g.12758408G=	GRCh37
NC_000019.8:g.12619408G=	NCBI36
NG_008318.1:g.24184C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2669C= MANE Select	ENSP00000395473.2:p.Ser890=
ENST00000221363.8:c.2666C=	ENSP00000221363.4:p.Ser889=
ENST00000456935.6:c.2669C=	ENSP00000395473.2:p.Ser890=
ENST00000466794.5:n.3259C=
ENST00000493218.5:n.80C=
ENST00000597692.1:c.228C=
NM_000528.3:c.2669C=	NP_000519.2:p.Ser890=
NM_001173498.1:c.2666C=	NP_001166969.1:p.Ser889=
XM_005259913.1:c.2672C=	XP_005259970.1:p.Ser891=
XM_011528017.1:c.1568C=	XP_011526319.1:p.Ser523=
XM_005259913.2:c.2672C=	XP_005259970.1:p.Ser891=
XM_024451518.1:c.1568C=	XP_024307286.1:p.Ser523=
NM_000528.4:c.2669C= MANE Select	NP_000519.2:p.Ser890=
NM_001173498.2:c.2666C=	NP_001166969.1:p.Ser889=