Canonical Allele Identifier: CA2323500145
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12650234C= , CM000681.2:g.12650234C= GRCh38
NC_000019.9:g.12761048C= , CM000681.1:g.12761048C= GRCh37
NC_000019.8:g.12622048C= NCBI36
NG_008318.1:g.21544G=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2047-12G= MANE Select ENSP00000395473.2:n.2047-12G=
ENST00000221363.8:c.2044-12G= ENSP00000221363.4:n.2044-12G=
ENST00000456935.6:c.2047-12G= ENSP00000395473.2:n.2047-12G=
ENST00000466794.5:n.2637-12G=
NM_000528.3:c.2047-12G= NP_000519.2:n.2047-12G=
NM_001173498.1:c.2044-12G= NP_001166969.1:n.2044-12G=
XM_005259913.1:c.2050-12G= XP_005259970.1:n.2050-12G=
XM_011528017.1:c.946-12G= XP_011526319.1:n.946-12G=
XM_005259913.2:c.2050-12G= XP_005259970.1:n.2050-12G=
XM_024451518.1:c.946-12G= XP_024307286.1:n.946-12G=
NM_000528.4:c.2047-12G= MANE Select NP_000519.2:n.2047-12G=
NM_001173498.2:c.2044-12G= NP_001166969.1:n.2044-12G=