Canonical Allele Identifier: CA1092125441
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1773949339
gnomAD v3: 6-96212142-G-A
gnomAD v4: 6-96212142-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212142G>A , CM000668.2:g.96212142G>A GRCh38
NC_000006.11:g.96660018G>A , CM000668.1:g.96660018G>A GRCh37
NC_000006.10:g.96766739G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.*7907G>A MANE Select ENSP00000302599.4:n.*7907G>A
ENST00000302103.5:c.*7907G>A ENSP00000302599.4:n.*7907G>A
NM_006581.3:c.*7907G>A NP_006572.2:n.*7907G>A
XR_942796.1:n.411-9127C>T
XR_942797.1:n.218-9127C>T
XR_942798.1:n.224-9127C>T
XR_942799.1:n.232-9127C>T
XR_942800.1:n.573-9127C>T
XM_011535383.2:c.*7907G>A XP_011533685.1:n.*7907G>A
XM_011535385.2:c.*7907G>A XP_011533687.1:n.*7907G>A
XM_017010188.1:c.*7907G>A XP_016865677.1:n.*7907G>A
XM_017010190.1:c.*7907G>A XP_016865679.1:n.*7907G>A
NM_006581.4:c.*7907G>A MANE Select NP_006572.2:n.*7907G>A