Canonical Allele Identifier: CA2340029939
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703262C= , CM000681.2:g.48703262C= GRCh38
NC_000019.9:g.49206519C= , CM000681.1:g.49206519C= GRCh37
NC_000019.8:g.53898331C= NCBI36
NG_007511.1:g.12292C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.306C= MANE Select ENSP00000387498.2:p.Thr102=
ENST00000522966.2:c.306C= ENSP00000430227.2:p.Thr102=
ENST00000391876.5:c.306C= ENSP00000375748.4:p.Thr102=
ENST00000425340.2:c.306C= ENSP00000387498.2:p.Thr102=
ENST00000522966.1:c.306C= ENSP00000430227.1:p.Thr102=
NM_000511.5:c.306C= NP_000502.4:p.Thr102=
NM_001097638.2:c.306C= NP_001091107.1:p.Thr102=
NR_131188.1:n.587G=
NM_000511.6:c.306C= MANE Select NP_000502.4:p.Thr102=
NM_001097638.3:c.306C= NP_001091107.1:p.Thr102=