Canonical Allele Identifier: CA2340030284
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703882A= , CM000681.2:g.48703882A= GRCh38
NC_000019.9:g.49207139A= , CM000681.1:g.49207139A= GRCh37
NC_000019.8:g.53898951A= NCBI36
NG_007511.1:g.12912A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.926A= MANE Select ENSP00000387498.2:p.Tyr309=
ENST00000522966.2:c.926A= ENSP00000430227.2:p.Tyr309=
ENST00000391876.5:c.926A= ENSP00000375748.4:p.Tyr309=
ENST00000425340.2:c.926A= ENSP00000387498.2:p.Tyr309=
NM_000511.5:c.926A= NP_000502.4:p.Tyr309=
NM_001097638.2:c.926A= NP_001091107.1:p.Tyr309=
NM_000511.6:c.926A= MANE Select NP_000502.4:p.Tyr309=
NM_001097638.3:c.926A= NP_001091107.1:p.Tyr309=