Canonical Allele Identifier: CA2340030058
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703468A= , CM000681.2:g.48703468A= GRCh38
NC_000019.9:g.49206725A= , CM000681.1:g.49206725A= GRCh37
NC_000019.8:g.53898537A= NCBI36
NG_007511.1:g.12498A=

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.512A= MANE Select ENSP00000387498.2:p.His171=
ENST00000522966.2:c.512A= ENSP00000430227.2:p.His171=
ENST00000391876.5:c.512A= ENSP00000375748.4:p.His171=
ENST00000425340.2:c.512A= ENSP00000387498.2:p.His171=
ENST00000522966.1:c.512A= ENSP00000430227.1:p.His171=
NM_000511.5:c.512A= NP_000502.4:p.His171=
NM_001097638.2:c.512A= NP_001091107.1:p.His171=
NR_131188.1:n.381T=
NM_000511.6:c.512A= MANE Select NP_000502.4:p.His171=
NM_001097638.3:c.512A= NP_001091107.1:p.His171=