Canonical Allele Identifier: CA406713212
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs1045864490

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703899C>G , CM000681.2:g.48703899C>G GRCh38
NC_000019.9:g.49207156C>G , CM000681.1:g.49207156C>G GRCh37
NC_000019.8:g.53898968C>G NCBI36
NG_007511.1:g.12929C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.943C>G MANE Select ENSP00000387498.2:p.Pro315Ala
ENST00000522966.2:c.943C>G ENSP00000430227.2:p.Pro315Ala
ENST00000391876.5:c.943C>G ENSP00000375748.4:p.Pro315Ala
ENST00000425340.2:c.943C>G ENSP00000387498.2:p.Pro315Ala
NM_000511.5:c.943C>G NP_000502.4:p.Pro315Ala
NM_001097638.2:c.943C>G NP_001091107.1:p.Pro315Ala
NM_000511.6:c.943C>G MANE Select NP_000502.4:p.Pro315Ala
NM_001097638.3:c.943C>G NP_001091107.1:p.Pro315Ala