Canonical Allele Identifier: CA568641185
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1413106814
gnomAD v2: 6-96505097-G-C
gnomAD v3: 6-96057221-G-C
gnomAD v4: 6-96057221-G-C
MyVariant Identifiers: chr6:g.96505097G>C (hg19) chr6:g.96057221G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057221G>C , CM000668.2:g.96057221G>C GRCh38
NC_000006.11:g.96505097G>C , CM000668.1:g.96505097G>C GRCh37
NC_000006.10:g.96611818G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41009G>C MANE Select ENSP00000302599.4:n.-98+41009G>C
ENST00000302103.5:c.-98+41009G>C ENSP00000302599.4:n.-98+41009G>C
NM_006581.3:c.-98+41009G>C NP_006572.2:n.-98+41009G>C
XM_011535384.1:c.-98+36248G>C XP_011533686.1:n.-98+36248G>C
XM_017010190.1:c.-215+41009G>C XP_016865679.1:n.-215+41009G>C
XR_001744267.2:n.2037C>G
NM_006581.4:c.-98+41009G>C MANE Select NP_006572.2:n.-98+41009G>C
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