Canonical Allele Identifier: CA406710887

Gene: FUT2

Linked Data

• dbSNP Id: rs2122223645
• MyVariant Identifiers: chr19:g.49206748C>A (hg19) ; chr19:g.48703491C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703491C>A , CM000681.2:g.48703491C>A	GRCh38
NC_000019.9:g.49206748C>A , CM000681.1:g.49206748C>A	GRCh37
NC_000019.8:g.53898560C>A	NCBI36
NG_007511.1:g.12521C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.535C>A MANE Select	ENSP00000387498.2:p.Gln179Lys
ENST00000522966.2:c.535C>A	ENSP00000430227.2:p.Gln179Lys
ENST00000391876.5:c.535C>A	ENSP00000375748.4:p.Gln179Lys
ENST00000425340.2:c.535C>A	ENSP00000387498.2:p.Gln179Lys
ENST00000522966.1:c.535C>A	ENSP00000430227.1:p.Gln179Lys
NM_000511.5:c.535C>A	NP_000502.4:p.Gln179Lys
NM_001097638.2:c.535C>A	NP_001091107.1:p.Gln179Lys
NR_131188.1:n.358G>T
NM_000511.6:c.535C>A MANE Select	NP_000502.4:p.Gln179Lys
NM_001097638.3:c.535C>A	NP_001091107.1:p.Gln179Lys