Canonical Allele Identifier: CA2323500099
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12650133T= , CM000681.2:g.12650133T= GRCh38
NC_000019.9:g.12760947T= , CM000681.1:g.12760947T= GRCh37
NC_000019.8:g.12621947T= NCBI36
NG_008318.1:g.21645A=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2136A= MANE Select ENSP00000395473.2:p.Leu712=
ENST00000221363.8:c.2133A= ENSP00000221363.4:p.Leu711=
ENST00000456935.6:c.2136A= ENSP00000395473.2:p.Leu712=
ENST00000466794.5:n.2726A=
NM_000528.3:c.2136A= NP_000519.2:p.Leu712=
NM_001173498.1:c.2133A= NP_001166969.1:p.Leu711=
XM_005259913.1:c.2139A= XP_005259970.1:p.Leu713=
XM_011528017.1:c.1035A= XP_011526319.1:p.Leu345=
XM_005259913.2:c.2139A= XP_005259970.1:p.Leu713=
XM_024451518.1:c.1035A= XP_024307286.1:p.Leu345=
NM_000528.4:c.2136A= MANE Select NP_000519.2:p.Leu712=
NM_001173498.2:c.2133A= NP_001166969.1:p.Leu711=