Canonical Allele Identifier: CA406711283
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs1456435064

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703567A>T , CM000681.2:g.48703567A>T GRCh38
NC_000019.9:g.49206824A>T , CM000681.1:g.49206824A>T GRCh37
NC_000019.8:g.53898636A>T NCBI36
NG_007511.1:g.12597A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.611A>T MANE Select ENSP00000387498.2:p.Asp204Val
ENST00000522966.2:c.611A>T ENSP00000430227.2:p.Asp204Val
ENST00000391876.5:c.611A>T ENSP00000375748.4:p.Asp204Val
ENST00000425340.2:c.611A>T ENSP00000387498.2:p.Asp204Val
ENST00000522966.1:c.611A>T ENSP00000430227.1:p.Asp204Val
NM_000511.5:c.611A>T NP_000502.4:p.Asp204Val
NM_001097638.2:c.611A>T NP_001091107.1:p.Asp204Val
NR_131188.1:n.282T>A
NM_000511.6:c.611A>T MANE Select NP_000502.4:p.Asp204Val
NM_001097638.3:c.611A>T NP_001091107.1:p.Asp204Val