Canonical Allele Identifier: CA2323498690

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647551C= , CM000681.2:g.12647551C=	GRCh38
NC_000019.9:g.12758365C= , CM000681.1:g.12758365C=	GRCh37
NC_000019.8:g.12619365C=	NCBI36
NG_008318.1:g.24227G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2712G= MANE Select	ENSP00000395473.2:p.Thr904=
ENST00000221363.8:c.2709G=	ENSP00000221363.4:p.Thr903=
ENST00000456935.6:c.2712G=	ENSP00000395473.2:p.Thr904=
ENST00000466794.5:n.3302G=
ENST00000469423.1:n.34G=
ENST00000493218.5:n.123G=
ENST00000597692.1:c.271G=
NM_000528.3:c.2712G=	NP_000519.2:p.Thr904=
NM_001173498.1:c.2709G=	NP_001166969.1:p.Thr903=
XM_005259913.1:c.2715G=	XP_005259970.1:p.Thr905=
XM_011528017.1:c.1611G=	XP_011526319.1:p.Thr537=
XM_005259913.2:c.2715G=	XP_005259970.1:p.Thr905=
XM_024451518.1:c.1611G=	XP_024307286.1:p.Thr537=
NM_000528.4:c.2712G= MANE Select	NP_000519.2:p.Thr904=
NM_001173498.2:c.2709G=	NP_001166969.1:p.Thr903=