Canonical Allele Identifier: CA508043223
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207176G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703919G>A , CM000681.2:g.48703919G>A GRCh38
NC_000019.9:g.49207176G>A , CM000681.1:g.49207176G>A GRCh37
NC_000019.8:g.53898988G>A NCBI36
NG_007511.1:g.12949G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.963G>A MANE Select ENSP00000387498.2:p.Lys321=
ENST00000522966.2:c.963G>A ENSP00000430227.2:p.Lys321=
ENST00000391876.5:c.963G>A ENSP00000375748.4:p.Lys321=
ENST00000425340.2:c.963G>A ENSP00000387498.2:p.Lys321=
NM_000511.5:c.963G>A NP_000502.4:p.Lys321=
NM_001097638.2:c.963G>A NP_001091107.1:p.Lys321=
NM_000511.6:c.963G>A MANE Select NP_000502.4:p.Lys321=
NM_001097638.3:c.963G>A NP_001091107.1:p.Lys321=