Canonical Allele Identifier: CA406712839
Gene: FUT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703828T>A , CM000681.2:g.48703828T>A GRCh38
NC_000019.9:g.49207085T>A , CM000681.1:g.49207085T>A GRCh37
NC_000019.8:g.53898897T>A NCBI36
NG_007511.1:g.12858T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.872T>A MANE Select ENSP00000387498.2:p.Phe291Tyr
ENST00000522966.2:c.872T>A ENSP00000430227.2:p.Phe291Tyr
ENST00000391876.5:c.872T>A ENSP00000375748.4:p.Phe291Tyr
ENST00000425340.2:c.872T>A ENSP00000387498.2:p.Phe291Tyr
NM_000511.5:c.872T>A NP_000502.4:p.Phe291Tyr
NM_001097638.2:c.872T>A NP_001091107.1:p.Phe291Tyr
NR_131188.1:n.21A>T
NM_000511.6:c.872T>A MANE Select NP_000502.4:p.Phe291Tyr
NM_001097638.3:c.872T>A NP_001091107.1:p.Phe291Tyr