Canonical Allele Identifier: CA508272543

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206519C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703262C>G , CM000681.2:g.48703262C>G	GRCh38
NC_000019.9:g.49206519C>G , CM000681.1:g.49206519C>G	GRCh37
NC_000019.8:g.53898331C>G	NCBI36
NG_007511.1:g.12292C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.306C>G MANE Select	ENSP00000387498.2:p.Thr102=
ENST00000522966.2:c.306C>G	ENSP00000430227.2:p.Thr102=
ENST00000391876.5:c.306C>G	ENSP00000375748.4:p.Thr102=
ENST00000425340.2:c.306C>G	ENSP00000387498.2:p.Thr102=
ENST00000522966.1:c.306C>G	ENSP00000430227.1:p.Thr102=
NM_000511.5:c.306C>G	NP_000502.4:p.Thr102=
NM_001097638.2:c.306C>G	NP_001091107.1:p.Thr102=
NR_131188.1:n.587G>C
NM_000511.6:c.306C>G MANE Select	NP_000502.4:p.Thr102=
NM_001097638.3:c.306C>G	NP_001091107.1:p.Thr102=