Canonical Allele Identifier: CA508272597

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206720C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703463C>T , CM000681.2:g.48703463C>T	GRCh38
NC_000019.9:g.49206720C>T , CM000681.1:g.49206720C>T	GRCh37
NC_000019.8:g.53898532C>T	NCBI36
NG_007511.1:g.12493C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000425340.3:c.507C>T MANE Select	ENSP00000387498.2:p.Thr169=
ENST00000522966.2:c.507C>T	ENSP00000430227.2:p.Thr169=
ENST00000391876.5:c.507C>T	ENSP00000375748.4:p.Thr169=
ENST00000425340.2:c.507C>T	ENSP00000387498.2:p.Thr169=
ENST00000522966.1:c.507C>T	ENSP00000430227.1:p.Thr169=
NM_000511.5:c.507C>T	NP_000502.4:p.Thr169=
NM_001097638.2:c.507C>T	NP_001091107.1:p.Thr169=
NR_131188.1:n.386G>A
NM_000511.6:c.507C>T MANE Select	NP_000502.4:p.Thr169=
NM_001097638.3:c.507C>T	NP_001091107.1:p.Thr169=