Canonical Allele Identifier: CA309352445
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs1800027

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703469C>G , CM000681.2:g.48703469C>G GRCh38
NC_000019.9:g.49206726C>G , CM000681.1:g.49206726C>G GRCh37
NC_000019.8:g.53898538C>G NCBI36
NG_007511.1:g.12499C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.513C>G MANE Select ENSP00000387498.2:p.His171Gln
ENST00000522966.2:c.513C>G ENSP00000430227.2:p.His171Gln
ENST00000391876.5:c.513C>G ENSP00000375748.4:p.His171Gln
ENST00000425340.2:c.513C>G ENSP00000387498.2:p.His171Gln
ENST00000522966.1:c.513C>G ENSP00000430227.1:p.His171Gln
NM_000511.5:c.513C>G NP_000502.4:p.His171Gln
NM_001097638.2:c.513C>G NP_001091107.1:p.His171Gln
NR_131188.1:n.380G>C
NM_000511.6:c.513C>G MANE Select NP_000502.4:p.His171Gln
NM_001097638.3:c.513C>G NP_001091107.1:p.His171Gln