Canonical Allele Identifier: CA2323506875
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12663706T= , CM000681.2:g.12663706T= GRCh38
NC_000019.9:g.12774520T= , CM000681.1:g.12774520T= GRCh37
NC_000019.8:g.12635520T= NCBI36
NG_008318.1:g.8072A=
NG_015814.1:g.1903T=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.760A= MANE Select ENSP00000395473.2:p.Thr254=
ENST00000221363.8:c.760A= ENSP00000221363.4:p.Thr254=
ENST00000456935.6:c.760A= ENSP00000395473.2:p.Thr254=
ENST00000466794.5:n.742A=
ENST00000486847.2:c.463A= ENSP00000470174.1:p.Thr155=
NM_000528.3:c.760A= NP_000519.2:p.Thr254=
NM_001173498.1:c.760A= NP_001166969.1:p.Thr254=
XM_005259913.1:c.760A= XP_005259970.1:p.Thr254=
XM_005259913.2:c.760A= XP_005259970.1:p.Thr254=
XM_024451518.1:c.-259A= XP_024307286.1:n.-259A=
NM_000528.4:c.760A= MANE Select NP_000519.2:p.Thr254=
NM_001173498.2:c.760A= NP_001166969.1:p.Thr254=