Canonical Allele Identifier: CA2323504065

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657937A= , CM000681.2:g.12657937A=	GRCh38
NC_000019.9:g.12768751A= , CM000681.1:g.12768751A=	GRCh37
NC_000019.8:g.12629751A=	NCBI36
NG_008318.1:g.13841T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1309+126T= MANE Select	ENSP00000395473.2:n.1309+126T=
ENST00000221363.8:c.1306+126T=	ENSP00000221363.4:n.1306+126T=
ENST00000456935.6:c.1309+126T=	ENSP00000395473.2:n.1309+126T=
ENST00000465830.1:n.473+126T=
ENST00000466794.5:n.1208+126T=
ENST00000495617.1:n.281-177T=
NM_000528.3:c.1309+126T=	NP_000519.2:n.1309+126T=
NM_001173498.1:c.1306+126T=	NP_001166969.1:n.1306+126T=
XM_005259913.1:c.1312+126T=	XP_005259970.1:n.1312+126T=
XM_011528017.1:c.208+126T=	XP_011526319.1:n.208+126T=
XM_005259913.2:c.1312+126T=	XP_005259970.1:n.1312+126T=
XM_024451518.1:c.208+126T=	XP_024307286.1:n.208+126T=
NM_000528.4:c.1309+126T= MANE Select	NP_000519.2:n.1309+126T=
NM_001173498.2:c.1306+126T=	NP_001166969.1:n.1306+126T=