Canonical Allele Identifier: CA2323504405
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12658489G= , CM000681.2:g.12658489G= GRCh38
NC_000019.9:g.12769303G= , CM000681.1:g.12769303G= GRCh37
NC_000019.8:g.12630303G= NCBI36
NG_008318.1:g.13289C=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.1048C= MANE Select ENSP00000395473.2:p.His350=
ENST00000221363.8:c.1045C= ENSP00000221363.4:p.His349=
ENST00000456935.6:c.1048C= ENSP00000395473.2:p.His350=
ENST00000465830.1:n.129C=
ENST00000466794.5:n.1009-145C=
ENST00000495617.1:n.280+242C=
NM_000528.3:c.1048C= NP_000519.2:p.His350=
NM_001173498.1:c.1045C= NP_001166969.1:p.His349=
XM_005259913.1:c.1051C= XP_005259970.1:p.His351=
XM_011528017.1:c.9-145C= XP_011526319.1:n.9-145C=
XM_005259913.2:c.1051C= XP_005259970.1:p.His351=
XM_024451518.1:c.9-145C= XP_024307286.1:n.9-145C=
NM_000528.4:c.1048C= MANE Select NP_000519.2:p.His350=
NM_001173498.2:c.1045C= NP_001166969.1:p.His349=