Canonical Allele Identifier: CA9556388
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs753287999
ExAC: 19:49207132 GC / G
gnomAD v2: 19-49207132-GC-G
MyVariant Identifiers: chr19:g.49207133del (hg19) chr19:g.48703876del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703877del , CM000681.2:g.48703877del GRCh38
NC_000019.9:g.49207134del , CM000681.1:g.49207134del GRCh37
NC_000019.8:g.53898946del NCBI36
NG_007511.1:g.12907del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.921del MANE Select ENSP00000387498.2:p.Asn308IlefsTer?
ENST00000522966.2:c.921del ENSP00000430227.2:p.Asn308IlefsTer?
ENST00000391876.5:c.921del ENSP00000375748.4:p.Asn308IlefsTer?
ENST00000425340.2:c.921del ENSP00000387498.2:p.Asn308IlefsTer?
NM_000511.5:c.921del NP_000502.4:p.Asn308IlefsTer?
NM_001097638.2:c.921del NP_001091107.1:p.Asn308IlefsTer?
NM_000511.6:c.921del MANE Select NP_000502.4:p.Asn308IlefsTer?
NM_001097638.3:c.921del NP_001091107.1:p.Asn308IlefsTer?
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