Canonical Allele Identifier: CA406708588

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206329G>A (hg19) ; chr19:g.48703072G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703072G>A , CM000681.2:g.48703072G>A	GRCh38
NC_000019.9:g.49206329G>A , CM000681.1:g.49206329G>A	GRCh37
NC_000019.8:g.53898141G>A	NCBI36
NG_007511.1:g.12102G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000425340.3:c.116G>A MANE Select	ENSP00000387498.2:p.Trp39Ter
ENST00000522966.2:c.116G>A	ENSP00000430227.2:p.Trp39Ter
ENST00000391876.5:c.116G>A	ENSP00000375748.4:p.Trp39Ter
ENST00000425340.2:c.116G>A	ENSP00000387498.2:p.Trp39Ter
ENST00000522966.1:c.116G>A	ENSP00000430227.1:p.Trp39Ter
NM_000511.5:c.116G>A	NP_000502.4:p.Trp39Ter
NM_001097638.2:c.116G>A	NP_001091107.1:p.Trp39Ter
NR_131188.1:n.777C>T
NM_000511.6:c.116G>A MANE Select	NP_000502.4:p.Trp39Ter
NM_001097638.3:c.116G>A	NP_001091107.1:p.Trp39Ter