Canonical Allele Identifier: CA1648570774
Gene: FUT9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057407C= , CM000668.2:g.96057407C= GRCh38
NC_000006.11:g.96505283C= , CM000668.1:g.96505283C= GRCh37
NC_000006.10:g.96612004C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41195C= MANE Select ENSP00000302599.4:n.-98+41195C=
ENST00000302103.5:c.-98+41195C= ENSP00000302599.4:n.-98+41195C=
NM_006581.3:c.-98+41195C= NP_006572.2:n.-98+41195C=
XM_011535384.1:c.-98+36434C= XP_011533686.1:n.-98+36434C=
XM_017010190.1:c.-215+41195C= XP_016865679.1:n.-215+41195C=
XR_001744267.2:n.1851G=
NM_006581.4:c.-98+41195C= MANE Select NP_006572.2:n.-98+41195C=
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