Canonical Allele Identifier: CA406713105
Gene: FUT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050189
ClinVar RCV Id: RCV001357223
dbSNP Id: rs1406380167
gnomAD v3: 19-48703879-A-G
gnomAD v4: 19-48703879-A-G
MyVariant Identifiers: chr19:g.49207136A>G (hg19) chr19:g.48703879A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703879A>G , CM000681.2:g.48703879A>G GRCh38
NC_000019.9:g.49207136A>G , CM000681.1:g.49207136A>G GRCh37
NC_000019.8:g.53898948A>G NCBI36
NG_007511.1:g.12909A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.923A>G MANE Select ENSP00000387498.2:p.Asn308Ser
ENST00000522966.2:c.923A>G ENSP00000430227.2:p.Asn308Ser
ENST00000391876.5:c.923A>G ENSP00000375748.4:p.Asn308Ser
ENST00000425340.2:c.923A>G ENSP00000387498.2:p.Asn308Ser
NM_000511.5:c.923A>G NP_000502.4:p.Asn308Ser
NM_001097638.2:c.923A>G NP_001091107.1:p.Asn308Ser
NM_000511.6:c.923A>G MANE Select NP_000502.4:p.Asn308Ser
NM_001097638.3:c.923A>G NP_001091107.1:p.Asn308Ser
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