Canonical Allele Identifier: CA2679725971
Gene: FUT9 HGNC NCBI

Linked Data

gnomAD v4: 6-96212176-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212176A>G , CM000668.2:g.96212176A>G GRCh38
NC_000006.11:g.96660052A>G , CM000668.1:g.96660052A>G GRCh37
NC_000006.10:g.96766773A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.*7941A>G MANE Select ENSP00000302599.4:n.*7941A>G
ENST00000302103.5:c.*7941A>G ENSP00000302599.4:n.*7941A>G
NM_006581.3:c.*7941A>G NP_006572.2:n.*7941A>G
XR_942796.1:n.411-9161T>C
XR_942797.1:n.218-9161T>C
XR_942798.1:n.224-9161T>C
XR_942799.1:n.232-9161T>C
XR_942800.1:n.573-9161T>C
XM_011535383.2:c.*7941A>G XP_011533685.1:n.*7941A>G
XM_011535385.2:c.*7941A>G XP_011533687.1:n.*7941A>G
XM_017010188.1:c.*7941A>G XP_016865677.1:n.*7941A>G
XM_017010190.1:c.*7941A>G XP_016865679.1:n.*7941A>G
NM_006581.4:c.*7941A>G MANE Select NP_006572.2:n.*7941A>G