Canonical Allele Identifier: CA2323498699

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647566C= , CM000681.2:g.12647566C=	GRCh38
NC_000019.9:g.12758380C= , CM000681.1:g.12758380C=	GRCh37
NC_000019.8:g.12619380C=	NCBI36
NG_008318.1:g.24212G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2697G= MANE Select	ENSP00000395473.2:p.Ser899=
ENST00000221363.8:c.2694G=	ENSP00000221363.4:p.Ser898=
ENST00000456935.6:c.2697G=	ENSP00000395473.2:p.Ser899=
ENST00000466794.5:n.3287G=
ENST00000469423.1:n.19G=
ENST00000493218.5:n.108G=
ENST00000597692.1:c.256G=
NM_000528.3:c.2697G=	NP_000519.2:p.Ser899=
NM_001173498.1:c.2694G=	NP_001166969.1:p.Ser898=
XM_005259913.1:c.2700G=	XP_005259970.1:p.Ser900=
XM_011528017.1:c.1596G=	XP_011526319.1:p.Ser532=
XM_005259913.2:c.2700G=	XP_005259970.1:p.Ser900=
XM_024451518.1:c.1596G=	XP_024307286.1:p.Ser532=
NM_000528.4:c.2697G= MANE Select	NP_000519.2:p.Ser899=
NM_001173498.2:c.2694G=	NP_001166969.1:p.Ser898=