Canonical Allele Identifier: CA2323498557

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647280T= , CM000681.2:g.12647280T=	GRCh38
NC_000019.9:g.12758094T= , CM000681.1:g.12758094T=	GRCh37
NC_000019.8:g.12619094T=	NCBI36
NG_008318.1:g.24498A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2876A= MANE Select	ENSP00000395473.2:p.Asn959=
ENST00000221363.8:c.2873A=	ENSP00000221363.4:p.Asn958=
ENST00000456935.6:c.2876A=	ENSP00000395473.2:p.Asn959=
ENST00000466794.5:n.3466A=
ENST00000469423.1:n.305A=
ENST00000493218.5:n.287A=
ENST00000597692.1:c.435A=
NM_000528.3:c.2876A=	NP_000519.2:p.Asn959=
NM_001173498.1:c.2873A=	NP_001166969.1:p.Asn958=
XM_005259913.1:c.2879A=	XP_005259970.1:p.Asn960=
XM_011528017.1:c.1775A=	XP_011526319.1:p.Asn592=
XM_005259913.2:c.2879A=	XP_005259970.1:p.Asn960=
XM_024451518.1:c.1775A=	XP_024307286.1:p.Asn592=
NM_000528.4:c.2876A= MANE Select	NP_000519.2:p.Asn959=
NM_001173498.2:c.2873A=	NP_001166969.1:p.Asn958=