Canonical Allele Identifier: CA913018672
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49206916del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703659del , CM000681.2:g.48703659del GRCh38
NC_000019.9:g.49206916del , CM000681.1:g.49206916del GRCh37
NC_000019.8:g.53898728del NCBI36
NG_007511.1:g.12689del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.703del MANE Select ENSP00000387498.2:p.Ser235AlafsTer?
ENST00000522966.2:c.703del ENSP00000430227.2:p.Ser235AlafsTer?
ENST00000391876.5:c.703del ENSP00000375748.4:p.Ser235AlafsTer?
ENST00000425340.2:c.703del ENSP00000387498.2:p.Ser235AlafsTer?
NM_000511.5:c.703del NP_000502.4:p.Ser235AlafsTer?
NM_001097638.2:c.703del NP_001091107.1:p.Ser235AlafsTer?
NR_131188.1:n.190del
NM_000511.6:c.703del MANE Select NP_000502.4:p.Ser235AlafsTer?
NM_001097638.3:c.703del NP_001091107.1:p.Ser235AlafsTer?