Canonical Allele Identifier: CA9556347
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs35398918
ExAC: 19:49206990 TGTG / T
gnomAD v2: 19-49206990-TGTG-T
gnomAD v3: 19-48703733-TGTG-T
gnomAD v4: 19-48703733-TGTG-T
MyVariant Identifiers: chr19:g.49206991_49206993del (hg19) chr19:g.48703734_48703736del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703737_48703739del , CM000681.2:g.48703737_48703739del GRCh38
NC_000019.9:g.49206994_49206996del , CM000681.1:g.49206994_49206996del GRCh37
NC_000019.8:g.53898806_53898808del NCBI36
NG_007511.1:g.12767_12769del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.781_783del MANE Select ENSP00000387498.2:p.Val261del
ENST00000522966.2:c.781_783del ENSP00000430227.2:p.Val261del
ENST00000391876.5:c.781_783del ENSP00000375748.4:p.Val261del
ENST00000425340.2:c.781_783del ENSP00000387498.2:p.Val261del
NM_000511.5:c.781_783del NP_000502.4:p.Val261del
NM_001097638.2:c.781_783del NP_001091107.1:p.Val261del
NR_131188.1:n.113_115del
NM_000511.6:c.781_783del MANE Select NP_000502.4:p.Val261del
NM_001097638.3:c.781_783del NP_001091107.1:p.Val261del
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