Canonical Allele Identifier: CA1092128269
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1770787697
gnomAD v3: 6-96057258-A-G
gnomAD v4: 6-96057258-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057258A>G , CM000668.2:g.96057258A>G GRCh38
NC_000006.11:g.96505134A>G , CM000668.1:g.96505134A>G GRCh37
NC_000006.10:g.96611855A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41046A>G MANE Select ENSP00000302599.4:n.-98+41046A>G
ENST00000302103.5:c.-98+41046A>G ENSP00000302599.4:n.-98+41046A>G
NM_006581.3:c.-98+41046A>G NP_006572.2:n.-98+41046A>G
XM_011535384.1:c.-98+36285A>G XP_011533686.1:n.-98+36285A>G
XM_017010190.1:c.-215+41046A>G XP_016865679.1:n.-215+41046A>G
XR_001744267.2:n.2000T>C
NM_006581.4:c.-98+41046A>G MANE Select NP_006572.2:n.-98+41046A>G