Canonical Allele Identifier: CA15425985
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs7745248
gnomAD v2: 6-96660114-G-A
gnomAD v3: 6-96212238-G-A
gnomAD v4: 6-96212238-G-A
MyVariant Identifiers: chr6:g.96660114G>A (hg19) chr6:g.96212238G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212238G>A , CM000668.2:g.96212238G>A GRCh38
NC_000006.11:g.96660114G>A , CM000668.1:g.96660114G>A GRCh37
NC_000006.10:g.96766835G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.*8003G>A MANE Select ENSP00000302599.4:n.*8003G>A
ENST00000302103.5:c.*8003G>A ENSP00000302599.4:n.*8003G>A
NM_006581.3:c.*8003G>A NP_006572.2:n.*8003G>A
XR_942796.1:n.411-9223C>T
XR_942797.1:n.218-9223C>T
XR_942798.1:n.224-9223C>T
XR_942799.1:n.232-9223C>T
XR_942800.1:n.573-9223C>T
XM_011535383.2:c.*8003G>A XP_011533685.1:n.*8003G>A
XM_011535385.2:c.*8003G>A XP_011533687.1:n.*8003G>A
XM_017010188.1:c.*8003G>A XP_016865677.1:n.*8003G>A
XM_017010190.1:c.*8003G>A XP_016865679.1:n.*8003G>A
NM_006581.4:c.*8003G>A MANE Select NP_006572.2:n.*8003G>A
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