Canonical Allele Identifier: CA406711131
Gene: FUT2 HGNC NCBI

Linked Data

gnomAD v4: 19-48703540-T-C
MyVariant Identifiers: chr19:g.49206797T>C (hg19) chr19:g.48703540T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703540T>C , CM000681.2:g.48703540T>C GRCh38
NC_000019.9:g.49206797T>C , CM000681.1:g.49206797T>C GRCh37
NC_000019.8:g.53898609T>C NCBI36
NG_007511.1:g.12570T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.584T>C MANE Select ENSP00000387498.2:p.Phe195Ser
ENST00000522966.2:c.584T>C ENSP00000430227.2:p.Phe195Ser
ENST00000391876.5:c.584T>C ENSP00000375748.4:p.Phe195Ser
ENST00000425340.2:c.584T>C ENSP00000387498.2:p.Phe195Ser
ENST00000522966.1:c.584T>C ENSP00000430227.1:p.Phe195Ser
NM_000511.5:c.584T>C NP_000502.4:p.Phe195Ser
NM_001097638.2:c.584T>C NP_001091107.1:p.Phe195Ser
NR_131188.1:n.309A>G
NM_000511.6:c.584T>C MANE Select NP_000502.4:p.Phe195Ser
NM_001097638.3:c.584T>C NP_001091107.1:p.Phe195Ser
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