Canonical Allele Identifier: CA2323504260

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658207G= , CM000681.2:g.12658207G=	GRCh38
NC_000019.9:g.12769021G= , CM000681.1:g.12769021G=	GRCh37
NC_000019.8:g.12630021G=	NCBI36
NG_008318.1:g.13571C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.1230+17C= MANE Select	ENSP00000395473.2:n.1230+17C=
ENST00000221363.8:c.1227+17C=	ENSP00000221363.4:n.1227+17C=
ENST00000456935.6:c.1230+17C=	ENSP00000395473.2:n.1230+17C=
ENST00000465830.1:n.394+17C=
ENST00000466794.5:n.1129+17C=
ENST00000495617.1:n.281-447C=
NM_000528.3:c.1230+17C=	NP_000519.2:n.1230+17C=
NM_001173498.1:c.1227+17C=	NP_001166969.1:n.1227+17C=
XM_005259913.1:c.1233+17C=	XP_005259970.1:n.1233+17C=
XM_011528017.1:c.129+17C=	XP_011526319.1:n.129+17C=
XM_005259913.2:c.1233+17C=	XP_005259970.1:n.1233+17C=
XM_024451518.1:c.129+17C=	XP_024307286.1:n.129+17C=
NM_000528.4:c.1230+17C= MANE Select	NP_000519.2:n.1230+17C=
NM_001173498.2:c.1227+17C=	NP_001166969.1:n.1227+17C=