Canonical Allele Identifier: CA568641189
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1202864816
gnomAD v2: 6-96505280-A-T
gnomAD v3: 6-96057404-A-T
gnomAD v4: 6-96057404-A-T
MyVariant Identifiers: chr6:g.96505280A>T (hg19) chr6:g.96057404A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057404A>T , CM000668.2:g.96057404A>T GRCh38
NC_000006.11:g.96505280A>T , CM000668.1:g.96505280A>T GRCh37
NC_000006.10:g.96612001A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+41192A>T MANE Select ENSP00000302599.4:n.-98+41192A>T
ENST00000302103.5:c.-98+41192A>T ENSP00000302599.4:n.-98+41192A>T
NM_006581.3:c.-98+41192A>T NP_006572.2:n.-98+41192A>T
XM_011535384.1:c.-98+36431A>T XP_011533686.1:n.-98+36431A>T
XM_017010190.1:c.-215+41192A>T XP_016865679.1:n.-215+41192A>T
XR_001744267.2:n.1854T>A
NM_006581.4:c.-98+41192A>T MANE Select NP_006572.2:n.-98+41192A>T
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