Canonical Allele Identifier: CA2323507710
Gene: MAN2B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12665435T= , CM000681.2:g.12665435T= GRCh38
NC_000019.9:g.12776249T= , CM000681.1:g.12776249T= GRCh37
NC_000019.8:g.12637249T= NCBI36
NG_008318.1:g.6343A=
NG_015814.1:g.3632T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.353A= MANE Select ENSP00000395473.2:p.Tyr118=
ENST00000221363.8:c.353A= ENSP00000221363.4:p.Tyr118=
ENST00000456935.6:c.353A= ENSP00000395473.2:p.Tyr118=
ENST00000466794.5:n.335A=
ENST00000486847.2:c.250A= ENSP00000470174.1:p.Thr84=
ENST00000596512.5:n.291A=
ENST00000597961.1:c.344A= ENSP00000472710.1:p.Tyr115=
ENST00000598876.1:c.380A= ENSP00000470533.1:p.Tyr127=
ENST00000600281.1:n.394A=
NM_000528.3:c.353A= NP_000519.2:p.Tyr118=
NM_001173498.1:c.353A= NP_001166969.1:p.Tyr118=
XM_005259913.1:c.353A= XP_005259970.1:p.Tyr118=
XM_005259913.2:c.353A= XP_005259970.1:p.Tyr118=
XM_024451518.1:c.-666A= XP_024307286.1:n.-666A=
NM_000528.4:c.353A= MANE Select NP_000519.2:p.Tyr118=
NM_001173498.2:c.353A= NP_001166969.1:p.Tyr118=