Canonical Allele Identifier: CA406711637
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs1453839552
gnomAD v2: 19-49206883-C-T
gnomAD v3: 19-48703626-C-T
gnomAD v4: 19-48703626-C-T
MyVariant Identifiers: chr19:g.49206883C>T (hg19) chr19:g.48703626C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703626C>T , CM000681.2:g.48703626C>T GRCh38
NC_000019.9:g.49206883C>T , CM000681.1:g.49206883C>T GRCh37
NC_000019.8:g.53898695C>T NCBI36
NG_007511.1:g.12656C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.670C>T MANE Select ENSP00000387498.2:p.Gln224Ter
ENST00000522966.2:c.670C>T ENSP00000430227.2:p.Gln224Ter
ENST00000391876.5:c.670C>T ENSP00000375748.4:p.Gln224Ter
ENST00000425340.2:c.670C>T ENSP00000387498.2:p.Gln224Ter
NM_000511.5:c.670C>T NP_000502.4:p.Gln224Ter
NM_001097638.2:c.670C>T NP_001091107.1:p.Gln224Ter
NR_131188.1:n.223G>A
NM_000511.6:c.670C>T MANE Select NP_000502.4:p.Gln224Ter
NM_001097638.3:c.670C>T NP_001091107.1:p.Gln224Ter
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