Canonical Allele Identifier: CA406712378

Gene: FUT2

Linked Data

• gnomAD v4: 19-48703731-G-T
• MyVariant Identifiers: chr19:g.49206988G>T (hg19) ; chr19:g.48703731G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703731G>T , CM000681.2:g.48703731G>T	GRCh38
NC_000019.9:g.49206988G>T , CM000681.1:g.49206988G>T	GRCh37
NC_000019.8:g.53898800G>T	NCBI36
NG_007511.1:g.12761G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.775G>T MANE Select	ENSP00000387498.2:p.Asp259Tyr
ENST00000522966.2:c.775G>T	ENSP00000430227.2:p.Asp259Tyr
ENST00000391876.5:c.775G>T	ENSP00000375748.4:p.Asp259Tyr
ENST00000425340.2:c.775G>T	ENSP00000387498.2:p.Asp259Tyr
NM_000511.5:c.775G>T	NP_000502.4:p.Asp259Tyr
NM_001097638.2:c.775G>T	NP_001091107.1:p.Asp259Tyr
NR_131188.1:n.118C>A
NM_000511.6:c.775G>T MANE Select	NP_000502.4:p.Asp259Tyr
NM_001097638.3:c.775G>T	NP_001091107.1:p.Asp259Tyr