Canonical Allele Identifier: CA9556287

Gene: FUT2

Linked Data

• dbSNP Id: rs766048744
• ExAC: 19:49206801 A / AG
• gnomAD v2: 19-49206801-A-AG
• gnomAD v3: 19-48703544-A-AG
• gnomAD v4: 19-48703544-A-AG
• MyVariant Identifiers: chr19:g.49206801_49206802insG (hg19) ; chr19:g.48703544_48703545insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703548dup , CM000681.2:g.48703548dup	GRCh38
NC_000019.9:g.49206805dup , CM000681.1:g.49206805dup	GRCh37
NC_000019.8:g.53898617dup	NCBI36
NG_007511.1:g.12578dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.592dup MANE Select	ENSP00000387498.2:p.Val198GlyfsTer?
ENST00000522966.2:c.592dup	ENSP00000430227.2:p.Val198GlyfsTer?
ENST00000391876.5:c.592dup	ENSP00000375748.4:p.Val198GlyfsTer?
ENST00000425340.2:c.592dup	ENSP00000387498.2:p.Val198GlyfsTer?
ENST00000522966.1:c.592dup	ENSP00000430227.1:p.Val198GlyfsTer?
NM_000511.5:c.592dup	NP_000502.4:p.Val198GlyfsTer?
NM_001097638.2:c.592dup	NP_001091107.1:p.Val198GlyfsTer?
NR_131188.1:n.304dup
NM_000511.6:c.592dup MANE Select	NP_000502.4:p.Val198GlyfsTer?
NM_001097638.3:c.592dup	NP_001091107.1:p.Val198GlyfsTer?