Canonical Allele Identifier: CA508272514
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207011C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703754C>A , CM000681.2:g.48703754C>A GRCh38
NC_000019.9:g.49207011C>A , CM000681.1:g.49207011C>A GRCh37
NC_000019.8:g.53898823C>A NCBI36
NG_007511.1:g.12784C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.798C>A MANE Select ENSP00000387498.2:p.Gly266=
ENST00000522966.2:c.798C>A ENSP00000430227.2:p.Gly266=
ENST00000391876.5:c.798C>A ENSP00000375748.4:p.Gly266=
ENST00000425340.2:c.798C>A ENSP00000387498.2:p.Gly266=
NM_000511.5:c.798C>A NP_000502.4:p.Gly266=
NM_001097638.2:c.798C>A NP_001091107.1:p.Gly266=
NR_131188.1:n.95G>T
NM_000511.6:c.798C>A MANE Select NP_000502.4:p.Gly266=
NM_001097638.3:c.798C>A NP_001091107.1:p.Gly266=
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