Canonical Allele Identifier: CA406713282
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207166A>T (hg19) chr19:g.48703909A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703909A>T , CM000681.2:g.48703909A>T GRCh38
NC_000019.9:g.49207166A>T , CM000681.1:g.49207166A>T GRCh37
NC_000019.8:g.53898978A>T NCBI36
NG_007511.1:g.12939A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.953A>T MANE Select ENSP00000387498.2:p.Lys318Ile
ENST00000522966.2:c.953A>T ENSP00000430227.2:p.Lys318Ile
ENST00000391876.5:c.953A>T ENSP00000375748.4:p.Lys318Ile
ENST00000425340.2:c.953A>T ENSP00000387498.2:p.Lys318Ile
NM_000511.5:c.953A>T NP_000502.4:p.Lys318Ile
NM_001097638.2:c.953A>T NP_001091107.1:p.Lys318Ile
NM_000511.6:c.953A>T MANE Select NP_000502.4:p.Lys318Ile
NM_001097638.3:c.953A>T NP_001091107.1:p.Lys318Ile
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