Canonical Allele Identifier: CA1648570669
Gene: FUT9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057172A= , CM000668.2:g.96057172A= GRCh38
NC_000006.11:g.96505048A= , CM000668.1:g.96505048A= GRCh37
NC_000006.10:g.96611769A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+40960A= MANE Select ENSP00000302599.4:n.-98+40960A=
ENST00000302103.5:c.-98+40960A= ENSP00000302599.4:n.-98+40960A=
NM_006581.3:c.-98+40960A= NP_006572.2:n.-98+40960A=
XM_011535384.1:c.-98+36199A= XP_011533686.1:n.-98+36199A=
XM_017010190.1:c.-215+40960A= XP_016865679.1:n.-215+40960A=
XR_001744267.2:n.2086T=
NM_006581.4:c.-98+40960A= MANE Select NP_006572.2:n.-98+40960A=
Search 100 bp 5'
Search 100 bp 3'