Canonical Allele Identifier: CA508272599
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49206723G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703466G>T , CM000681.2:g.48703466G>T GRCh38
NC_000019.9:g.49206723G>T , CM000681.1:g.49206723G>T GRCh37
NC_000019.8:g.53898535G>T NCBI36
NG_007511.1:g.12496G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.510G>T MANE Select ENSP00000387498.2:p.Leu170=
ENST00000522966.2:c.510G>T ENSP00000430227.2:p.Leu170=
ENST00000391876.5:c.510G>T ENSP00000375748.4:p.Leu170=
ENST00000425340.2:c.510G>T ENSP00000387498.2:p.Leu170=
ENST00000522966.1:c.510G>T ENSP00000430227.1:p.Leu170=
NM_000511.5:c.510G>T NP_000502.4:p.Leu170=
NM_001097638.2:c.510G>T NP_001091107.1:p.Leu170=
NR_131188.1:n.383C>A
NM_000511.6:c.510G>T MANE Select NP_000502.4:p.Leu170=
NM_001097638.3:c.510G>T NP_001091107.1:p.Leu170=