Canonical Allele Identifier: CA508272505
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207002T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703745T>G , CM000681.2:g.48703745T>G GRCh38
NC_000019.9:g.49207002T>G , CM000681.1:g.49207002T>G GRCh37
NC_000019.8:g.53898814T>G NCBI36
NG_007511.1:g.12775T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.789T>G MANE Select ENSP00000387498.2:p.Ala263=
ENST00000522966.2:c.789T>G ENSP00000430227.2:p.Ala263=
ENST00000391876.5:c.789T>G ENSP00000375748.4:p.Ala263=
ENST00000425340.2:c.789T>G ENSP00000387498.2:p.Ala263=
NM_000511.5:c.789T>G NP_000502.4:p.Ala263=
NM_001097638.2:c.789T>G NP_001091107.1:p.Ala263=
NR_131188.1:n.104A>C
NM_000511.6:c.789T>G MANE Select NP_000502.4:p.Ala263=
NM_001097638.3:c.789T>G NP_001091107.1:p.Ala263=