Canonical Allele Identifier: CA2323503663

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657297C= , CM000681.2:g.12657297C=	GRCh38
NC_000019.9:g.12768111C= , CM000681.1:g.12768111C=	GRCh37
NC_000019.8:g.12629111C=	NCBI36
NG_008318.1:g.14481G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1419+149G= MANE Select	ENSP00000395473.2:n.1419+149G=
ENST00000221363.8:c.1416+149G=	ENSP00000221363.4:n.1416+149G=
ENST00000456935.6:c.1419+149G=	ENSP00000395473.2:n.1419+149G=
ENST00000466794.5:n.1318+149G=
ENST00000495617.1:n.595+149G=
ENST00000593686.1:c.29+149G=
ENST00000595880.5:n.16+67G=
NM_000528.3:c.1419+149G=	NP_000519.2:n.1419+149G=
NM_001173498.1:c.1416+149G=	NP_001166969.1:n.1416+149G=
XM_005259913.1:c.1422+149G=	XP_005259970.1:n.1422+149G=
XM_011528017.1:c.318+149G=	XP_011526319.1:n.318+149G=
XM_005259913.2:c.1422+149G=	XP_005259970.1:n.1422+149G=
XM_024451518.1:c.318+149G=	XP_024307286.1:n.318+149G=
NM_000528.4:c.1419+149G= MANE Select	NP_000519.2:n.1419+149G=
NM_001173498.2:c.1416+149G=	NP_001166969.1:n.1416+149G=