Canonical Allele Identifier: CA2323505740
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12661357T= , CM000681.2:g.12661357T= GRCh38
NC_000019.9:g.12772171T= , CM000681.1:g.12772171T= GRCh37
NC_000019.8:g.12633171T= NCBI36
NG_008318.1:g.10421A=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.929A= MANE Select ENSP00000395473.2:p.Asn310=
ENST00000221363.8:c.929A= ENSP00000221363.4:p.Asn310=
ENST00000456935.6:c.929A= ENSP00000395473.2:p.Asn310=
ENST00000462144.1:n.122A=
ENST00000466794.5:n.911A=
NM_000528.3:c.929A= NP_000519.2:p.Asn310=
NM_001173498.1:c.929A= NP_001166969.1:p.Asn310=
XM_005259913.1:c.929A= XP_005259970.1:p.Asn310=
XM_011528017.1:c.-90A= XP_011526319.1:n.-90A=
XM_005259913.2:c.929A= XP_005259970.1:p.Asn310=
XM_024451518.1:c.-90A= XP_024307286.1:n.-90A=
NM_000528.4:c.929A= MANE Select NP_000519.2:p.Asn310=
NM_001173498.2:c.929A= NP_001166969.1:p.Asn310=