Canonical Allele Identifier: CA144130520
Gene: FUT9 HGNC NCBI
COSMIC:
COSN14947634 (not active)
MyVariant.info:
GRCh38 chr6:g.96111973C>T
GRCh37 chr6:g.96559849C>T
gnomAD v2:
6:96559849 C / T
gnomAD v3:
6:96111973 C / T
gnomAD v4:
chr6-96111973-C-T
Joint Max Group AF 0.59024133 (EAS)
Genomes Max Group AF 0.59024133 (EAS)
dbSNP:
3811070
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96111973C>T , CM000668.2:g.96111973C>T GRCh38
NC_000006.11:g.96559849C>T , CM000668.1:g.96559849C>T GRCh37
NC_000006.10:g.96666570C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-97-2066C>T MANE Select ENSP00000302599.4:n.-97-2066C>T
ENST00000302103.5:c.-97-2066C>T ENSP00000302599.4:n.-97-2066C>T
NM_006581.3:c.-97-2066C>T NP_006572.2:n.-97-2066C>T
XM_011535383.1:c.-98+1175C>T XP_011533685.1:n.-98+1175C>T
XM_011535384.1:c.-97-2066C>T XP_011533686.1:n.-97-2066C>T
XM_011535385.1:c.-215+1175C>T XP_011533687.1:n.-215+1175C>T
XM_011535383.2:c.-98+1175C>T XP_011533685.1:n.-98+1175C>T
XM_011535385.2:c.-215+1175C>T XP_011533687.1:n.-215+1175C>T
XM_017010188.1:c.-98+1175C>T XP_016865677.1:n.-98+1175C>T
XM_017010190.1:c.-214-2066C>T XP_016865679.1:n.-214-2066C>T
NM_006581.4:c.-97-2066C>T MANE Select NP_006572.2:n.-97-2066C>T
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