Canonical Allele Identifier: CA2323499581

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649208G= , CM000681.2:g.12649208G=	GRCh38
NC_000019.9:g.12760022G= , CM000681.1:g.12760022G=	GRCh37
NC_000019.8:g.12621022G=	NCBI36
NG_008318.1:g.22570C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2364C= MANE Select	ENSP00000395473.2:p.Asn788=
ENST00000221363.8:c.2361C=	ENSP00000221363.4:p.Asn787=
ENST00000456935.6:c.2364C=	ENSP00000395473.2:p.Asn788=
ENST00000466794.5:n.2954C=
NM_000528.3:c.2364C=	NP_000519.2:p.Asn788=
NM_001173498.1:c.2361C=	NP_001166969.1:p.Asn787=
XM_005259913.1:c.2367C=	XP_005259970.1:p.Asn789=
XM_011528017.1:c.1263C=	XP_011526319.1:p.Asn421=
XM_005259913.2:c.2367C=	XP_005259970.1:p.Asn789=
XM_024451518.1:c.1263C=	XP_024307286.1:p.Asn421=
NM_000528.4:c.2364C= MANE Select	NP_000519.2:p.Asn788=
NM_001173498.2:c.2361C=	NP_001166969.1:p.Asn787=