Canonical Allele Identifier: CA144124237
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs541230363
gnomAD v3: 6-96057388-G-A
gnomAD v4: 6-96057388-G-A
MyVariant Identifiers: chr6:g.96505264G>A (hg19) chr6:g.96057388G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057388G>A , CM000668.2:g.96057388G>A GRCh38
NC_000006.11:g.96505264G>A , CM000668.1:g.96505264G>A GRCh37
NC_000006.10:g.96611985G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41176G>A MANE Select ENSP00000302599.4:n.-98+41176G>A
ENST00000302103.5:c.-98+41176G>A ENSP00000302599.4:n.-98+41176G>A
NM_006581.3:c.-98+41176G>A NP_006572.2:n.-98+41176G>A
XM_011535384.1:c.-98+36415G>A XP_011533686.1:n.-98+36415G>A
XM_017010190.1:c.-215+41176G>A XP_016865679.1:n.-215+41176G>A
XR_001744267.2:n.1870C>T
NM_006581.4:c.-98+41176G>A MANE Select NP_006572.2:n.-98+41176G>A
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