Canonical Allele Identifier: CA2340030034
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs2032563355

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703423_48703425del , CM000681.2:g.48703423_48703425del GRCh38
NC_000019.9:g.49206680_49206682del , CM000681.1:g.49206680_49206682del GRCh37
NC_000019.8:g.53898492_53898494del NCBI36
NG_007511.1:g.12453_12455del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.467_469del MANE Select ENSP00000387498.2:p.Phe156del
ENST00000522966.2:c.467_469del ENSP00000430227.2:p.Phe156del
ENST00000391876.5:c.467_469del ENSP00000375748.4:p.Phe156del
ENST00000425340.2:c.467_469del ENSP00000387498.2:p.Phe156del
ENST00000522966.1:c.467_469del ENSP00000430227.1:p.Phe156del
NM_000511.5:c.467_469del NP_000502.4:p.Phe156del
NM_001097638.2:c.467_469del NP_001091107.1:p.Phe156del
NR_131188.1:n.426_428del
NM_000511.6:c.467_469del MANE Select NP_000502.4:p.Phe156del
NM_001097638.3:c.467_469del NP_001091107.1:p.Phe156del