Canonical Allele Identifier: CA406708661
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs577430628
MyVariant Identifiers: chr19:g.49206345G>C (hg19) chr19:g.48703088G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703088G>C , CM000681.2:g.48703088G>C GRCh38
NC_000019.9:g.49206345G>C , CM000681.1:g.49206345G>C GRCh37
NC_000019.8:g.53898157G>C NCBI36
NG_007511.1:g.12118G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.132G>C MANE Select ENSP00000387498.2:p.Gln44His
ENST00000522966.2:c.132G>C ENSP00000430227.2:p.Gln44His
ENST00000391876.5:c.132G>C ENSP00000375748.4:p.Gln44His
ENST00000425340.2:c.132G>C ENSP00000387498.2:p.Gln44His
ENST00000522966.1:c.132G>C ENSP00000430227.1:p.Gln44His
NM_000511.5:c.132G>C NP_000502.4:p.Gln44His
NM_001097638.2:c.132G>C NP_001091107.1:p.Gln44His
NR_131188.1:n.761C>G
NM_000511.6:c.132G>C MANE Select NP_000502.4:p.Gln44His
NM_001097638.3:c.132G>C NP_001091107.1:p.Gln44His
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