Canonical Allele Identifier: CA406711409

Gene: FUT2

Linked Data

• COSMIC: COSM5094413
• MyVariant Identifiers: chr19:g.49206847G>A (hg19) ; chr19:g.48703590G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703590G>A , CM000681.2:g.48703590G>A	GRCh38
NC_000019.9:g.49206847G>A , CM000681.1:g.49206847G>A	GRCh37
NC_000019.8:g.53898659G>A	NCBI36
NG_007511.1:g.12620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.634G>A MANE Select	ENSP00000387498.2:p.Val212Met
ENST00000522966.2:c.634G>A	ENSP00000430227.2:p.Val212Met
ENST00000391876.5:c.634G>A	ENSP00000375748.4:p.Val212Met
ENST00000425340.2:c.634G>A	ENSP00000387498.2:p.Val212Met
ENST00000522966.1:c.634G>A	ENSP00000430227.1:p.Val212Met
NM_000511.5:c.634G>A	NP_000502.4:p.Val212Met
NM_001097638.2:c.634G>A	NP_001091107.1:p.Val212Met
NR_131188.1:n.259C>T
NM_000511.6:c.634G>A MANE Select	NP_000502.4:p.Val212Met
NM_001097638.3:c.634G>A	NP_001091107.1:p.Val212Met