Canonical Allele Identifier: CA2340030272
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703863A= , CM000681.2:g.48703863A= GRCh38
NC_000019.9:g.49207120A= , CM000681.1:g.49207120A= GRCh37
NC_000019.8:g.53898932A= NCBI36
NG_007511.1:g.12893A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.907A= MANE Select ENSP00000387498.2:p.Thr303=
ENST00000522966.2:c.907A= ENSP00000430227.2:p.Thr303=
ENST00000391876.5:c.907A= ENSP00000375748.4:p.Thr303=
ENST00000425340.2:c.907A= ENSP00000387498.2:p.Thr303=
NM_000511.5:c.907A= NP_000502.4:p.Thr303=
NM_001097638.2:c.907A= NP_001091107.1:p.Thr303=
NM_000511.6:c.907A= MANE Select NP_000502.4:p.Thr303=
NM_001097638.3:c.907A= NP_001091107.1:p.Thr303=