Canonical Allele Identifier: CA2323503800

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657494C= , CM000681.2:g.12657494C=	GRCh38
NC_000019.9:g.12768308C= , CM000681.1:g.12768308C=	GRCh37
NC_000019.8:g.12629308C=	NCBI36
NG_008318.1:g.14284G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1371G= MANE Select	ENSP00000395473.2:p.Val457=
ENST00000221363.8:c.1368G=	ENSP00000221363.4:p.Val456=
ENST00000456935.6:c.1371G=	ENSP00000395473.2:p.Val457=
ENST00000465830.1:n.535G=
ENST00000466794.5:n.1270G=
ENST00000495617.1:n.547G=
NM_000528.3:c.1371G=	NP_000519.2:p.Val457=
NM_001173498.1:c.1368G=	NP_001166969.1:p.Val456=
XM_005259913.1:c.1374G=	XP_005259970.1:p.Val458=
XM_011528017.1:c.270G=	XP_011526319.1:p.Val90=
XM_005259913.2:c.1374G=	XP_005259970.1:p.Val458=
XM_024451518.1:c.270G=	XP_024307286.1:p.Val90=
NM_000528.4:c.1371G= MANE Select	NP_000519.2:p.Val457=
NM_001173498.2:c.1368G=	NP_001166969.1:p.Val456=