Canonical Allele Identifier: CA1648570785
Gene: FUT9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057426T= , CM000668.2:g.96057426T= GRCh38
NC_000006.11:g.96505302T= , CM000668.1:g.96505302T= GRCh37
NC_000006.10:g.96612023T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+41214T= MANE Select ENSP00000302599.4:n.-98+41214T=
ENST00000302103.5:c.-98+41214T= ENSP00000302599.4:n.-98+41214T=
NM_006581.3:c.-98+41214T= NP_006572.2:n.-98+41214T=
XM_011535384.1:c.-98+36453T= XP_011533686.1:n.-98+36453T=
XM_017010190.1:c.-215+41214T= XP_016865679.1:n.-215+41214T=
XR_001744267.2:n.1832A=
NM_006581.4:c.-98+41214T= MANE Select NP_006572.2:n.-98+41214T=
Search 100 bp 5'
Search 100 bp 3'