Canonical Allele Identifier: CA2323505741
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12661359G= , CM000681.2:g.12661359G= GRCh38
NC_000019.9:g.12772173G= , CM000681.1:g.12772173G= GRCh37
NC_000019.8:g.12633173G= NCBI36
NG_008318.1:g.10419C=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.927C= MANE Select ENSP00000395473.2:p.Thr309=
ENST00000221363.8:c.927C= ENSP00000221363.4:p.Thr309=
ENST00000456935.6:c.927C= ENSP00000395473.2:p.Thr309=
ENST00000462144.1:n.120C=
ENST00000466794.5:n.909C=
NM_000528.3:c.927C= NP_000519.2:p.Thr309=
NM_001173498.1:c.927C= NP_001166969.1:p.Thr309=
XM_005259913.1:c.927C= XP_005259970.1:p.Thr309=
XM_011528017.1:c.-92C= XP_011526319.1:n.-92C=
XM_005259913.2:c.927C= XP_005259970.1:p.Thr309=
XM_024451518.1:c.-92C= XP_024307286.1:n.-92C=
NM_000528.4:c.927C= MANE Select NP_000519.2:p.Thr309=
NM_001173498.2:c.927C= NP_001166969.1:p.Thr309=