Canonical Allele Identifier: CA406711294

Gene: FUT2

Linked Data

• gnomAD v4: 19-48703569-T-C
• MyVariant Identifiers: chr19:g.49206826T>C (hg19) ; chr19:g.48703569T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703569T>C , CM000681.2:g.48703569T>C	GRCh38
NC_000019.9:g.49206826T>C , CM000681.1:g.49206826T>C	GRCh37
NC_000019.8:g.53898638T>C	NCBI36
NG_007511.1:g.12599T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000425340.3:c.613T>C MANE Select	ENSP00000387498.2:p.Tyr205His
ENST00000522966.2:c.613T>C	ENSP00000430227.2:p.Tyr205His
ENST00000391876.5:c.613T>C	ENSP00000375748.4:p.Tyr205His
ENST00000425340.2:c.613T>C	ENSP00000387498.2:p.Tyr205His
ENST00000522966.1:c.613T>C	ENSP00000430227.1:p.Tyr205His
NM_000511.5:c.613T>C	NP_000502.4:p.Tyr205His
NM_001097638.2:c.613T>C	NP_001091107.1:p.Tyr205His
NR_131188.1:n.280A>G
NM_000511.6:c.613T>C MANE Select	NP_000502.4:p.Tyr205His
NM_001097638.3:c.613T>C	NP_001091107.1:p.Tyr205His