Canonical Allele Identifier: CA568641184
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1177336527
gnomAD v2: 6-96505066-AT-A
MyVariant Identifiers: chr6:g.96505067del (hg19) chr6:g.96057191del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057192del , CM000668.2:g.96057192del GRCh38
NC_000006.11:g.96505068del , CM000668.1:g.96505068del GRCh37
NC_000006.10:g.96611789del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+40980del MANE Select ENSP00000302599.4:n.-98+40980del
ENST00000302103.5:c.-98+40980del ENSP00000302599.4:n.-98+40980del
NM_006581.3:c.-98+40980del NP_006572.2:n.-98+40980del
XM_011535384.1:c.-98+36219del XP_011533686.1:n.-98+36219del
XM_017010190.1:c.-215+40980del XP_016865679.1:n.-215+40980del
XR_001744267.2:n.2067del
NM_006581.4:c.-98+40980del MANE Select NP_006572.2:n.-98+40980del
Search 100 bp 5'
Search 100 bp 3'