Canonical Allele Identifier: CA122800
Gene: FUT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12946
ClinVar RCV Id: RCV000013811
dbSNP Id: rs1047781

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703374A>T , CM000681.2:g.48703374A>T GRCh38
NC_000019.9:g.49206631A>T , CM000681.1:g.49206631A>T GRCh37
NC_000019.8:g.53898443A>T NCBI36
NG_007511.1:g.12404A>T

Transcript Alleles

HGVS Amino-acid change
NM_000511.5:c.418A>T VV NP_000502.4:p.Ile140Phe
NM_001097638.2:c.418A>T VV NP_001091107.1:p.Ile140Phe
NR_131188.1:n.475T>A
ENST00000391876.5:c.418A>T ENSP00000375748.4:p.Ile140Phe
ENST00000425340.2:c.418A>T ENSP00000387498.2:p.Ile140Phe
ENST00000522966.1:c.418A>T ENSP00000430227.1:p.Ile140Phe