Canonical Allele Identifier: CA1648570740
Gene: FUT9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057329T= , CM000668.2:g.96057329T= GRCh38
NC_000006.11:g.96505205T= , CM000668.1:g.96505205T= GRCh37
NC_000006.10:g.96611926T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+41117T= MANE Select ENSP00000302599.4:n.-98+41117T=
ENST00000302103.5:c.-98+41117T= ENSP00000302599.4:n.-98+41117T=
NM_006581.3:c.-98+41117T= NP_006572.2:n.-98+41117T=
XM_011535384.1:c.-98+36356T= XP_011533686.1:n.-98+36356T=
XM_017010190.1:c.-215+41117T= XP_016865679.1:n.-215+41117T=
XR_001744267.2:n.1929A=
NM_006581.4:c.-98+41117T= MANE Select NP_006572.2:n.-98+41117T=
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