Canonical Allele Identifier: CA2323500100
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12650138C= , CM000681.2:g.12650138C= GRCh38
NC_000019.9:g.12760952C= , CM000681.1:g.12760952C= GRCh37
NC_000019.8:g.12621952C= NCBI36
NG_008318.1:g.21640G=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2131G= MANE Select ENSP00000395473.2:p.Glu711=
ENST00000221363.8:c.2128G= ENSP00000221363.4:p.Glu710=
ENST00000456935.6:c.2131G= ENSP00000395473.2:p.Glu711=
ENST00000466794.5:n.2721G=
NM_000528.3:c.2131G= NP_000519.2:p.Glu711=
NM_001173498.1:c.2128G= NP_001166969.1:p.Glu710=
XM_005259913.1:c.2134G= XP_005259970.1:p.Glu712=
XM_011528017.1:c.1030G= XP_011526319.1:p.Glu344=
XM_005259913.2:c.2134G= XP_005259970.1:p.Glu712=
XM_024451518.1:c.1030G= XP_024307286.1:p.Glu344=
NM_000528.4:c.2131G= MANE Select NP_000519.2:p.Glu711=
NM_001173498.2:c.2128G= NP_001166969.1:p.Glu710=