Canonical Allele Identifier: CA2323498612
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12647390T= , CM000681.2:g.12647390T= GRCh38
NC_000019.9:g.12758204T= , CM000681.1:g.12758204T= GRCh37
NC_000019.8:g.12619204T= NCBI36
NG_008318.1:g.24388A=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2820+53A= MANE Select ENSP00000395473.2:n.2820+53A=
ENST00000221363.8:c.2817+53A= ENSP00000221363.4:n.2817+53A=
ENST00000456935.6:c.2820+53A= ENSP00000395473.2:n.2820+53A=
ENST00000466794.5:n.3410+53A=
ENST00000469423.1:n.195A=
ENST00000493218.5:n.231+53A=
ENST00000597692.1:c.379+53A=
NM_000528.3:c.2820+53A= NP_000519.2:n.2820+53A=
NM_001173498.1:c.2817+53A= NP_001166969.1:n.2817+53A=
XM_005259913.1:c.2823+53A= XP_005259970.1:n.2823+53A=
XM_011528017.1:c.1719+53A= XP_011526319.1:n.1719+53A=
XM_005259913.2:c.2823+53A= XP_005259970.1:n.2823+53A=
XM_024451518.1:c.1719+53A= XP_024307286.1:n.1719+53A=
NM_000528.4:c.2820+53A= MANE Select NP_000519.2:n.2820+53A=
NM_001173498.2:c.2817+53A= NP_001166969.1:n.2817+53A=