Canonical Allele Identifier: CA404246471
Gene: MAN2B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12657040G>C , CM000681.2:g.12657040G>C GRCh38
NC_000019.9:g.12767854G>C , CM000681.1:g.12767854G>C GRCh37
NC_000019.8:g.12628854G>C NCBI36
NG_008318.1:g.14738C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.1436C>G MANE Select ENSP00000395473.2:p.Ala479Gly
ENST00000221363.8:c.1433C>G ENSP00000221363.4:p.Ala478Gly
ENST00000433513.5:n.42C>G
ENST00000456935.6:c.1436C>G ENSP00000395473.2:p.Ala479Gly
ENST00000466794.5:n.1335C>G
ENST00000495617.1:n.612C>G
ENST00000593686.1:c.46C>G
ENST00000595880.5:n.33C>G
NM_000528.3:c.1436C>G NP_000519.2:p.Ala479Gly
NM_001173498.1:c.1433C>G NP_001166969.1:p.Ala478Gly
XM_005259913.1:c.1439C>G XP_005259970.1:p.Ala480Gly
XM_011528017.1:c.335C>G XP_011526319.1:p.Ala112Gly
XM_005259913.2:c.1439C>G XP_005259970.1:p.Ala480Gly
XM_024451518.1:c.335C>G XP_024307286.1:p.Ala112Gly
NM_000528.4:c.1436C>G MANE Select NP_000519.2:p.Ala479Gly
NM_001173498.2:c.1433C>G NP_001166969.1:p.Ala478Gly