Canonical Allele Identifier: CA9556374
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs141630650
ExAC: 19:49207101 A / C
gnomAD v2: 19-49207101-A-C
gnomAD v3: 19-48703844-A-C
gnomAD v4: 19-48703844-A-C
MyVariant Identifiers: chr19:g.49207101A>C (hg19) chr19:g.48703844A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703844A>C , CM000681.2:g.48703844A>C GRCh38
NC_000019.9:g.49207101A>C , CM000681.1:g.49207101A>C GRCh37
NC_000019.8:g.53898913A>C NCBI36
NG_007511.1:g.12874A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.888A>C MANE Select ENSP00000387498.2:p.Ala296=
ENST00000522966.2:c.888A>C ENSP00000430227.2:p.Ala296=
ENST00000391876.5:c.888A>C ENSP00000375748.4:p.Ala296=
ENST00000425340.2:c.888A>C ENSP00000387498.2:p.Ala296=
NM_000511.5:c.888A>C NP_000502.4:p.Ala296=
NM_001097638.2:c.888A>C NP_001091107.1:p.Ala296=
NR_131188.1:n.5T>G
NM_000511.6:c.888A>C MANE Select NP_000502.4:p.Ala296=
NM_001097638.3:c.888A>C NP_001091107.1:p.Ala296=
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Search 100 bp 3'