Canonical Allele Identifier: CA404243334
Gene: MAN2B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12650157G>C , CM000681.2:g.12650157G>C GRCh38
NC_000019.9:g.12760971G>C , CM000681.1:g.12760971G>C GRCh37
NC_000019.8:g.12621971G>C NCBI36
NG_008318.1:g.21621C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.2112C>G MANE Select ENSP00000395473.2:p.Tyr704Ter
ENST00000221363.8:c.2109C>G ENSP00000221363.4:p.Tyr703Ter
ENST00000456935.6:c.2112C>G ENSP00000395473.2:p.Tyr704Ter
ENST00000466794.5:n.2702C>G
NM_000528.3:c.2112C>G NP_000519.2:p.Tyr704Ter
NM_001173498.1:c.2109C>G NP_001166969.1:p.Tyr703Ter
XM_005259913.1:c.2115C>G XP_005259970.1:p.Tyr705Ter
XM_011528017.1:c.1011C>G XP_011526319.1:p.Tyr337Ter
XM_005259913.2:c.2115C>G XP_005259970.1:p.Tyr705Ter
XM_024451518.1:c.1011C>G XP_024307286.1:p.Tyr337Ter
NM_000528.4:c.2112C>G MANE Select NP_000519.2:p.Tyr704Ter
NM_001173498.2:c.2109C>G NP_001166969.1:p.Tyr703Ter