Canonical Allele Identifier: CA2323499550
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12649141G= , CM000681.2:g.12649141G= GRCh38
NC_000019.9:g.12759955G= , CM000681.1:g.12759955G= GRCh37
NC_000019.8:g.12620955G= NCBI36
NG_008318.1:g.22637C=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2431C= MANE Select ENSP00000395473.2:p.Leu811=
ENST00000221363.8:c.2428C= ENSP00000221363.4:p.Leu810=
ENST00000456935.6:c.2431C= ENSP00000395473.2:p.Leu811=
ENST00000466794.5:n.3021C=
NM_000528.3:c.2431C= NP_000519.2:p.Leu811=
NM_001173498.1:c.2428C= NP_001166969.1:p.Leu810=
XM_005259913.1:c.2434C= XP_005259970.1:p.Leu812=
XM_011528017.1:c.1330C= XP_011526319.1:p.Leu444=
XM_005259913.2:c.2434C= XP_005259970.1:p.Leu812=
XM_024451518.1:c.1330C= XP_024307286.1:p.Leu444=
NM_000528.4:c.2431C= MANE Select NP_000519.2:p.Leu811=
NM_001173498.2:c.2428C= NP_001166969.1:p.Leu810=