Canonical Allele Identifier: CA1648570795
Gene: FUT9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057454A= , CM000668.2:g.96057454A= GRCh38
NC_000006.11:g.96505330A= , CM000668.1:g.96505330A= GRCh37
NC_000006.10:g.96612051A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+41242A= MANE Select ENSP00000302599.4:n.-98+41242A=
ENST00000302103.5:c.-98+41242A= ENSP00000302599.4:n.-98+41242A=
NM_006581.3:c.-98+41242A= NP_006572.2:n.-98+41242A=
XM_011535384.1:c.-98+36481A= XP_011533686.1:n.-98+36481A=
XM_017010190.1:c.-215+41242A= XP_016865679.1:n.-215+41242A=
XR_001744267.2:n.1804T=
NM_006581.4:c.-98+41242A= MANE Select NP_006572.2:n.-98+41242A=
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