Canonical Allele Identifier: CA2323498774

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647649A= , CM000681.2:g.12647649A=	GRCh38
NC_000019.9:g.12758463A= , CM000681.1:g.12758463A=	GRCh37
NC_000019.8:g.12619463A=	NCBI36
NG_008318.1:g.24129T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2665-51T= MANE Select	ENSP00000395473.2:n.2665-51T=
ENST00000221363.8:c.2662-51T=	ENSP00000221363.4:n.2662-51T=
ENST00000456935.6:c.2665-51T=	ENSP00000395473.2:n.2665-51T=
ENST00000466794.5:n.3255-51T=
ENST00000493218.5:n.25T=
ENST00000597692.1:c.224-51T=
NM_000528.3:c.2665-51T=	NP_000519.2:n.2665-51T=
NM_001173498.1:c.2662-51T=	NP_001166969.1:n.2662-51T=
XM_005259913.1:c.2668-51T=	XP_005259970.1:n.2668-51T=
XM_011528017.1:c.1564-51T=	XP_011526319.1:n.1564-51T=
XM_005259913.2:c.2668-51T=	XP_005259970.1:n.2668-51T=
XM_024451518.1:c.1564-51T=	XP_024307286.1:n.1564-51T=
NM_000528.4:c.2665-51T= MANE Select	NP_000519.2:n.2665-51T=
NM_001173498.2:c.2662-51T=	NP_001166969.1:n.2662-51T=