Canonical Allele Identifier: CA830114753
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1191003175
gnomAD v3: 6-96057309-C-T
gnomAD v4: 6-96057309-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057309C>T , CM000668.2:g.96057309C>T GRCh38
NC_000006.11:g.96505185C>T , CM000668.1:g.96505185C>T GRCh37
NC_000006.10:g.96611906C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41097C>T MANE Select ENSP00000302599.4:n.-98+41097C>T
ENST00000302103.5:c.-98+41097C>T ENSP00000302599.4:n.-98+41097C>T
NM_006581.3:c.-98+41097C>T NP_006572.2:n.-98+41097C>T
XM_011535384.1:c.-98+36336C>T XP_011533686.1:n.-98+36336C>T
XM_017010190.1:c.-215+41097C>T XP_016865679.1:n.-215+41097C>T
XR_001744267.2:n.1949G>A
NM_006581.4:c.-98+41097C>T MANE Select NP_006572.2:n.-98+41097C>T