Canonical Allele Identifier: CA2323507674

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665361C= , CM000681.2:g.12665361C=	GRCh38
NC_000019.9:g.12776175C= , CM000681.1:g.12776175C=	GRCh37
NC_000019.8:g.12637175C=	NCBI36
NG_008318.1:g.6417G=
NG_015814.1:g.3558C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.427G= MANE Select	ENSP00000395473.2:p.Val143=
ENST00000221363.8:c.427G=	ENSP00000221363.4:p.Val143=
ENST00000456935.6:c.427G=	ENSP00000395473.2:p.Val143=
ENST00000466794.5:n.409G=
ENST00000486847.2:c.324G=	ENSP00000470174.1:p.Leu108=
ENST00000596512.5:n.365G=
ENST00000597961.1:c.418G=	ENSP00000472710.1:p.Val140=
ENST00000598876.1:c.454G=	ENSP00000470533.1:p.Val152=
ENST00000600281.1:n.468G=
NM_000528.3:c.427G=	NP_000519.2:p.Val143=
NM_001173498.1:c.427G=	NP_001166969.1:p.Val143=
XM_005259913.1:c.427G=	XP_005259970.1:p.Val143=
XM_005259913.2:c.427G=	XP_005259970.1:p.Val143=
XM_024451518.1:c.-592G=	XP_024307286.1:n.-592G=
NM_000528.4:c.427G= MANE Select	NP_000519.2:p.Val143=
NM_001173498.2:c.427G=	NP_001166969.1:p.Val143=