Canonical Allele Identifier: CA9556121
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs772734604
ExAC: 19:49206232 C / A
gnomAD v2: 19-49206232-C-A
gnomAD v3: 19-48702975-C-A
gnomAD v4: 19-48702975-C-A
MyVariant Identifiers: chr19:g.49206232C>A (hg19) chr19:g.48702975C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48702975C>A , CM000681.2:g.48702975C>A GRCh38
NC_000019.9:g.49206232C>A , CM000681.1:g.49206232C>A GRCh37
NC_000019.8:g.53898044C>A NCBI36
NG_007511.1:g.12005C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000425340.3:c.19C>A MANE Select ENSP00000387498.2:p.Pro7Thr
ENST00000522966.2:c.19C>A ENSP00000430227.2:p.Pro7Thr
ENST00000391876.5:c.19C>A ENSP00000375748.4:p.Pro7Thr
ENST00000425340.2:c.19C>A ENSP00000387498.2:p.Pro7Thr
ENST00000522966.1:c.19C>A ENSP00000430227.1:p.Pro7Thr
NM_000511.5:c.19C>A NP_000502.4:p.Pro7Thr
NM_001097638.2:c.19C>A NP_001091107.1:p.Pro7Thr
NR_131188.1:n.874G>T
NM_000511.6:c.19C>A MANE Select NP_000502.4:p.Pro7Thr
NM_001097638.3:c.19C>A NP_001091107.1:p.Pro7Thr
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