Canonical Allele Identifier: CA2340030239
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703806A= , CM000681.2:g.48703806A= GRCh38
NC_000019.9:g.49207063A= , CM000681.1:g.49207063A= GRCh37
NC_000019.8:g.53898875A= NCBI36
NG_007511.1:g.12836A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.850A= MANE Select ENSP00000387498.2:p.Thr284=
ENST00000522966.2:c.850A= ENSP00000430227.2:p.Thr284=
ENST00000391876.5:c.850A= ENSP00000375748.4:p.Thr284=
ENST00000425340.2:c.850A= ENSP00000387498.2:p.Thr284=
NM_000511.5:c.850A= NP_000502.4:p.Thr284=
NM_001097638.2:c.850A= NP_001091107.1:p.Thr284=
NR_131188.1:n.43T=
NM_000511.6:c.850A= MANE Select NP_000502.4:p.Thr284=
NM_001097638.3:c.850A= NP_001091107.1:p.Thr284=