Canonical Allele Identifier: CA406712159
Gene: FUT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703696C>A , CM000681.2:g.48703696C>A GRCh38
NC_000019.9:g.49206953C>A , CM000681.1:g.49206953C>A GRCh37
NC_000019.8:g.53898765C>A NCBI36
NG_007511.1:g.12726C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.740C>A MANE Select ENSP00000387498.2:p.Ala247Asp
ENST00000522966.2:c.740C>A ENSP00000430227.2:p.Ala247Asp
ENST00000391876.5:c.740C>A ENSP00000375748.4:p.Ala247Asp
ENST00000425340.2:c.740C>A ENSP00000387498.2:p.Ala247Asp
NM_000511.5:c.740C>A NP_000502.4:p.Ala247Asp
NM_001097638.2:c.740C>A NP_001091107.1:p.Ala247Asp
NR_131188.1:n.153G>T
NM_000511.6:c.740C>A MANE Select NP_000502.4:p.Ala247Asp
NM_001097638.3:c.740C>A NP_001091107.1:p.Ala247Asp