Canonical Allele Identifier: CA2340030130
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703575C= , CM000681.2:g.48703575C= GRCh38
NC_000019.9:g.49206832C= , CM000681.1:g.49206832C= GRCh37
NC_000019.8:g.53898644C= NCBI36
NG_007511.1:g.12605C=

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.619C= MANE Select ENSP00000387498.2:p.His207=
ENST00000522966.2:c.619C= ENSP00000430227.2:p.His207=
ENST00000391876.5:c.619C= ENSP00000375748.4:p.His207=
ENST00000425340.2:c.619C= ENSP00000387498.2:p.His207=
ENST00000522966.1:c.619C= ENSP00000430227.1:p.His207=
NM_000511.5:c.619C= NP_000502.4:p.His207=
NM_001097638.2:c.619C= NP_001091107.1:p.His207=
NR_131188.1:n.274G=
NM_000511.6:c.619C= MANE Select NP_000502.4:p.His207=
NM_001097638.3:c.619C= NP_001091107.1:p.His207=