Canonical Allele Identifier: CA2323507859
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12665753G= , CM000681.2:g.12665753G= GRCh38
NC_000019.9:g.12776567G= , CM000681.1:g.12776567G= GRCh37
NC_000019.8:g.12637567G= NCBI36
NG_008318.1:g.6025C=
NG_015814.1:g.3950G=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.212C= MANE Select ENSP00000395473.2:p.Thr71=
ENST00000221363.8:c.212C= ENSP00000221363.4:p.Thr71=
ENST00000456935.6:c.212C= ENSP00000395473.2:p.Thr71=
ENST00000466794.5:n.194C=
ENST00000486847.2:c.160-228C= ENSP00000470174.1:n.160-228C=
ENST00000596512.5:n.201-228C=
ENST00000597961.1:c.203C= ENSP00000472710.1:p.Thr68=
ENST00000598876.1:c.239C= ENSP00000470533.1:p.Thr80=
ENST00000600281.1:n.253C=
NM_000528.3:c.212C= NP_000519.2:p.Thr71=
NM_001173498.1:c.212C= NP_001166969.1:p.Thr71=
XM_005259913.1:c.212C= XP_005259970.1:p.Thr71=
XM_005259913.2:c.212C= XP_005259970.1:p.Thr71=
XM_024451518.1:c.-807C= XP_024307286.1:n.-807C=
NM_000528.4:c.212C= MANE Select NP_000519.2:p.Thr71=
NM_001173498.2:c.212C= NP_001166969.1:p.Thr71=