Canonical Allele Identifier: CA9556350
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs550360759
ExAC: 19:49207005 C / A
gnomAD v2: 19-49207005-C-A
gnomAD v3: 19-48703748-C-A
gnomAD v4: 19-48703748-C-A
MyVariant Identifiers: chr19:g.49207005C>A (hg19) chr19:g.48703748C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703748C>A , CM000681.2:g.48703748C>A GRCh38
NC_000019.9:g.49207005C>A , CM000681.1:g.49207005C>A GRCh37
NC_000019.8:g.53898817C>A NCBI36
NG_007511.1:g.12778C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.792C>A MANE Select ENSP00000387498.2:p.Gly264=
ENST00000522966.2:c.792C>A ENSP00000430227.2:p.Gly264=
ENST00000391876.5:c.792C>A ENSP00000375748.4:p.Gly264=
ENST00000425340.2:c.792C>A ENSP00000387498.2:p.Gly264=
NM_000511.5:c.792C>A NP_000502.4:p.Gly264=
NM_001097638.2:c.792C>A NP_001091107.1:p.Gly264=
NR_131188.1:n.101G>T
NM_000511.6:c.792C>A MANE Select NP_000502.4:p.Gly264=
NM_001097638.3:c.792C>A NP_001091107.1:p.Gly264=
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