Canonical Allele Identifier: CA2323498652
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12647467G= , CM000681.2:g.12647467G= GRCh38
NC_000019.9:g.12758281G= , CM000681.1:g.12758281G= GRCh37
NC_000019.8:g.12619281G= NCBI36
NG_008318.1:g.24311C=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2796C= MANE Select ENSP00000395473.2:p.Ser932=
ENST00000221363.8:c.2793C= ENSP00000221363.4:p.Ser931=
ENST00000456935.6:c.2796C= ENSP00000395473.2:p.Ser932=
ENST00000466794.5:n.3386C=
ENST00000469423.1:n.118C=
ENST00000493218.5:n.207C=
ENST00000597692.1:c.355C=
NM_000528.3:c.2796C= NP_000519.2:p.Ser932=
NM_001173498.1:c.2793C= NP_001166969.1:p.Ser931=
XM_005259913.1:c.2799C= XP_005259970.1:p.Ser933=
XM_011528017.1:c.1695C= XP_011526319.1:p.Ser565=
XM_005259913.2:c.2799C= XP_005259970.1:p.Ser933=
XM_024451518.1:c.1695C= XP_024307286.1:p.Ser565=
NM_000528.4:c.2796C= MANE Select NP_000519.2:p.Ser932=
NM_001173498.2:c.2793C= NP_001166969.1:p.Ser931=