Canonical Allele Identifier: CA406713395
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207177C>T (hg19) chr19:g.48703920C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703920C>T , CM000681.2:g.48703920C>T GRCh38
NC_000019.9:g.49207177C>T , CM000681.1:g.49207177C>T GRCh37
NC_000019.8:g.53898989C>T NCBI36
NG_007511.1:g.12950C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.964C>T MANE Select ENSP00000387498.2:p.Pro322Ser
ENST00000522966.2:c.964C>T ENSP00000430227.2:p.Pro322Ser
ENST00000391876.5:c.964C>T ENSP00000375748.4:p.Pro322Ser
ENST00000425340.2:c.964C>T ENSP00000387498.2:p.Pro322Ser
NM_000511.5:c.964C>T NP_000502.4:p.Pro322Ser
NM_001097638.2:c.964C>T NP_001091107.1:p.Pro322Ser
NM_000511.6:c.964C>T MANE Select NP_000502.4:p.Pro322Ser
NM_001097638.3:c.964C>T NP_001091107.1:p.Pro322Ser
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