Canonical Allele Identifier: CA406710660

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206707T>A (hg19) ; chr19:g.48703450T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703450T>A , CM000681.2:g.48703450T>A	GRCh38
NC_000019.9:g.49206707T>A , CM000681.1:g.49206707T>A	GRCh37
NC_000019.8:g.53898519T>A	NCBI36
NG_007511.1:g.12480T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.494T>A MANE Select	ENSP00000387498.2:p.Leu165His
ENST00000522966.2:c.494T>A	ENSP00000430227.2:p.Leu165His
ENST00000391876.5:c.494T>A	ENSP00000375748.4:p.Leu165His
ENST00000425340.2:c.494T>A	ENSP00000387498.2:p.Leu165His
ENST00000522966.1:c.494T>A	ENSP00000430227.1:p.Leu165His
NM_000511.5:c.494T>A	NP_000502.4:p.Leu165His
NM_001097638.2:c.494T>A	NP_001091107.1:p.Leu165His
NR_131188.1:n.399A>T
NM_000511.6:c.494T>A MANE Select	NP_000502.4:p.Leu165His
NM_001097638.3:c.494T>A	NP_001091107.1:p.Leu165His