Canonical Allele Identifier: CA2323502871

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12655845T= , CM000681.2:g.12655845T=	GRCh38
NC_000019.9:g.12766659T= , CM000681.1:g.12766659T=	GRCh37
NC_000019.8:g.12627659T=	NCBI36
NG_008318.1:g.15933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1679A= MANE Select	ENSP00000395473.2:p.His560=
ENST00000221363.8:c.1676A=	ENSP00000221363.4:p.His559=
ENST00000433513.5:n.285A=
ENST00000456935.6:c.1679A=	ENSP00000395473.2:p.His560=
ENST00000466794.5:n.2269A=
ENST00000593686.1:c.272A=
ENST00000595880.5:n.276A=
ENST00000596591.1:c.43A=
NM_000528.3:c.1679A=	NP_000519.2:p.His560=
NM_001173498.1:c.1676A=	NP_001166969.1:p.His559=
XM_005259913.1:c.1682A=	XP_005259970.1:p.His561=
XM_011528017.1:c.578A=	XP_011526319.1:p.His193=
XM_005259913.2:c.1682A=	XP_005259970.1:p.His561=
XM_024451518.1:c.578A=	XP_024307286.1:p.His193=
NM_000528.4:c.1679A= MANE Select	NP_000519.2:p.His560=
NM_001173498.2:c.1676A=	NP_001166969.1:p.His559=