Canonical Allele Identifier: CA2323505692

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12661252G= , CM000681.2:g.12661252G=	GRCh38
NC_000019.9:g.12772066G= , CM000681.1:g.12772066G=	GRCh37
NC_000019.8:g.12633066G=	NCBI36
NG_008318.1:g.10526C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.1026+8C= MANE Select	ENSP00000395473.2:n.1026+8C=
ENST00000221363.8:c.1026+8C=	ENSP00000221363.4:n.1026+8C=
ENST00000456935.6:c.1026+8C=	ENSP00000395473.2:n.1026+8C=
ENST00000462144.1:n.227C=
ENST00000466794.5:n.1008+8C=
NM_000528.3:c.1026+8C=	NP_000519.2:n.1026+8C=
NM_001173498.1:c.1026+8C=	NP_001166969.1:n.1026+8C=
XM_005259913.1:c.1026+8C=	XP_005259970.1:n.1026+8C=
XM_011528017.1:c.8+8C=	XP_011526319.1:n.8+8C=
XM_005259913.2:c.1026+8C=	XP_005259970.1:n.1026+8C=
XM_024451518.1:c.8+8C=	XP_024307286.1:n.8+8C=
NM_000528.4:c.1026+8C= MANE Select	NP_000519.2:n.1026+8C=
NM_001173498.2:c.1026+8C=	NP_001166969.1:n.1026+8C=