Canonical Allele Identifier: CA2323499593
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12649233G= , CM000681.2:g.12649233G= GRCh38
NC_000019.9:g.12760047G= , CM000681.1:g.12760047G= GRCh37
NC_000019.8:g.12621047G= NCBI36
NG_008318.1:g.22545C=

Transcript Alleles

HGVS Amino-acid change
ENST00000456935.7:c.2356-17C= MANE Select ENSP00000395473.2:n.2356-17C=
ENST00000221363.8:c.2353-17C= ENSP00000221363.4:n.2353-17C=
ENST00000456935.6:c.2356-17C= ENSP00000395473.2:n.2356-17C=
ENST00000466794.5:n.2946-17C=
NM_000528.3:c.2356-17C= NP_000519.2:n.2356-17C=
NM_001173498.1:c.2353-17C= NP_001166969.1:n.2353-17C=
XM_005259913.1:c.2359-17C= XP_005259970.1:n.2359-17C=
XM_011528017.1:c.1255-17C= XP_011526319.1:n.1255-17C=
XM_005259913.2:c.2359-17C= XP_005259970.1:n.2359-17C=
XM_024451518.1:c.1255-17C= XP_024307286.1:n.1255-17C=
NM_000528.4:c.2356-17C= MANE Select NP_000519.2:n.2356-17C=
NM_001173498.2:c.2353-17C= NP_001166969.1:n.2353-17C=