Canonical Allele Identifier: CA508043061
Gene: FUT2 HGNC NCBI

Linked Data

gnomAD v4: 19-48703874-G-A
MyVariant Identifiers: chr19:g.49207131G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703874G>A , CM000681.2:g.48703874G>A GRCh38
NC_000019.9:g.49207131G>A , CM000681.1:g.49207131G>A GRCh37
NC_000019.8:g.53898943G>A NCBI36
NG_007511.1:g.12904G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.918G>A MANE Select ENSP00000387498.2:p.Leu306=
ENST00000522966.2:c.918G>A ENSP00000430227.2:p.Leu306=
ENST00000391876.5:c.918G>A ENSP00000375748.4:p.Leu306=
ENST00000425340.2:c.918G>A ENSP00000387498.2:p.Leu306=
NM_000511.5:c.918G>A NP_000502.4:p.Leu306=
NM_001097638.2:c.918G>A NP_001091107.1:p.Leu306=
NM_000511.6:c.918G>A MANE Select NP_000502.4:p.Leu306=
NM_001097638.3:c.918G>A NP_001091107.1:p.Leu306=
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