Canonical Allele Identifier: CA9556344

Gene: FUT2

Linked Data

• ClinVar Variation Id: 996599
• ClinVar RCV Id: RCV001291127 ; RCV003316837
• dbSNP Id: rs602662
• ExAC: 19:49206985 G / A
• gnomAD v2: 19-49206985-G-A
• gnomAD v3: 19-48703728-G-A
• gnomAD v4: 19-48703728-G-A
• MyVariant Identifiers: chr19:g.49206985G>A (hg19) ; chr19:g.48703728G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703728G>A , CM000681.2:g.48703728G>A	GRCh38
NC_000019.9:g.49206985G>A , CM000681.1:g.49206985G>A	GRCh37
NC_000019.8:g.53898797G>A	NCBI36
NG_007511.1:g.12758G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.772G>A MANE Select	ENSP00000387498.2:p.Gly258Ser
ENST00000522966.2:c.772G>A	ENSP00000430227.2:p.Gly258Ser
ENST00000391876.5:c.772G>A	ENSP00000375748.4:p.Gly258Ser
ENST00000425340.2:c.772G>A	ENSP00000387498.2:p.Gly258Ser
NM_000511.5:c.772G>A	NP_000502.4:p.Gly258Ser
NM_001097638.2:c.772G>A	NP_001091107.1:p.Gly258Ser
NR_131188.1:n.121C>T
NM_000511.6:c.772G>A MANE Select	NP_000502.4:p.Gly258Ser
NM_001097638.3:c.772G>A	NP_001091107.1:p.Gly258Ser