Canonical Allele Identifier: CA508272194
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49206817C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703560C>A , CM000681.2:g.48703560C>A GRCh38
NC_000019.9:g.49206817C>A , CM000681.1:g.49206817C>A GRCh37
NC_000019.8:g.53898629C>A NCBI36
NG_007511.1:g.12590C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.604C>A MANE Select ENSP00000387498.2:p.Arg202=
ENST00000522966.2:c.604C>A ENSP00000430227.2:p.Arg202=
ENST00000391876.5:c.604C>A ENSP00000375748.4:p.Arg202=
ENST00000425340.2:c.604C>A ENSP00000387498.2:p.Arg202=
ENST00000522966.1:c.604C>A ENSP00000430227.1:p.Arg202=
NM_000511.5:c.604C>A NP_000502.4:p.Arg202=
NM_001097638.2:c.604C>A NP_001091107.1:p.Arg202=
NR_131188.1:n.289G>T
NM_000511.6:c.604C>A MANE Select NP_000502.4:p.Arg202=
NM_001097638.3:c.604C>A NP_001091107.1:p.Arg202=