Canonical Allele Identifier: CA508042829
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207050A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703793A>T , CM000681.2:g.48703793A>T GRCh38
NC_000019.9:g.49207050A>T , CM000681.1:g.49207050A>T GRCh37
NC_000019.8:g.53898862A>T NCBI36
NG_007511.1:g.12823A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.837A>T MANE Select ENSP00000387498.2:p.Thr279=
ENST00000522966.2:c.837A>T ENSP00000430227.2:p.Thr279=
ENST00000391876.5:c.837A>T ENSP00000375748.4:p.Thr279=
ENST00000425340.2:c.837A>T ENSP00000387498.2:p.Thr279=
NM_000511.5:c.837A>T NP_000502.4:p.Thr279=
NM_001097638.2:c.837A>T NP_001091107.1:p.Thr279=
NR_131188.1:n.56T>A
NM_000511.6:c.837A>T MANE Select NP_000502.4:p.Thr279=
NM_001097638.3:c.837A>T NP_001091107.1:p.Thr279=