Canonical Allele Identifier: CA309352482

Gene: FUT2

Linked Data

• dbSNP Id: rs1012932049
• gnomAD v2: 19-49206809-A-G
• gnomAD v3: 19-48703552-A-G
• gnomAD v4: 19-48703552-A-G
• MyVariant Identifiers: chr19:g.49206809A>G (hg19) ; chr19:g.48703552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703552A>G , CM000681.2:g.48703552A>G	GRCh38
NC_000019.9:g.49206809A>G , CM000681.1:g.49206809A>G	GRCh37
NC_000019.8:g.53898621A>G	NCBI36
NG_007511.1:g.12582A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.596A>G MANE Select	ENSP00000387498.2:p.His199Arg
ENST00000522966.2:c.596A>G	ENSP00000430227.2:p.His199Arg
ENST00000391876.5:c.596A>G	ENSP00000375748.4:p.His199Arg
ENST00000425340.2:c.596A>G	ENSP00000387498.2:p.His199Arg
ENST00000522966.1:c.596A>G	ENSP00000430227.1:p.His199Arg
NM_000511.5:c.596A>G	NP_000502.4:p.His199Arg
NM_001097638.2:c.596A>G	NP_001091107.1:p.His199Arg
NR_131188.1:n.297T>C
NM_000511.6:c.596A>G MANE Select	NP_000502.4:p.His199Arg
NM_001097638.3:c.596A>G	NP_001091107.1:p.His199Arg