Canonical Allele Identifier: CA508272560

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49207038T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703781T>C , CM000681.2:g.48703781T>C	GRCh38
NC_000019.9:g.49207038T>C , CM000681.1:g.49207038T>C	GRCh37
NC_000019.8:g.53898850T>C	NCBI36
NG_007511.1:g.12811T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.825T>C MANE Select	ENSP00000387498.2:p.Phe275=
ENST00000522966.2:c.825T>C	ENSP00000430227.2:p.Phe275=
ENST00000391876.5:c.825T>C	ENSP00000375748.4:p.Phe275=
ENST00000425340.2:c.825T>C	ENSP00000387498.2:p.Phe275=
NM_000511.5:c.825T>C	NP_000502.4:p.Phe275=
NM_001097638.2:c.825T>C	NP_001091107.1:p.Phe275=
NR_131188.1:n.68A>G
NM_000511.6:c.825T>C MANE Select	NP_000502.4:p.Phe275=
NM_001097638.3:c.825T>C	NP_001091107.1:p.Phe275=