Canonical Allele Identifier: CA1648673459
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1773949540

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212165A>C , CM000668.2:g.96212165A>C GRCh38
NC_000006.11:g.96660041A>C , CM000668.1:g.96660041A>C GRCh37
NC_000006.10:g.96766762A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.*7930A>C MANE Select ENSP00000302599.4:n.*7930A>C
ENST00000302103.5:c.*7930A>C ENSP00000302599.4:n.*7930A>C
NM_006581.3:c.*7930A>C NP_006572.2:n.*7930A>C
XR_942796.1:n.411-9150T>G
XR_942797.1:n.218-9150T>G
XR_942798.1:n.224-9150T>G
XR_942799.1:n.232-9150T>G
XR_942800.1:n.573-9150T>G
XM_011535383.2:c.*7930A>C XP_011533685.1:n.*7930A>C
XM_011535385.2:c.*7930A>C XP_011533687.1:n.*7930A>C
XM_017010188.1:c.*7930A>C XP_016865677.1:n.*7930A>C
XM_017010190.1:c.*7930A>C XP_016865679.1:n.*7930A>C
NM_006581.4:c.*7930A>C MANE Select NP_006572.2:n.*7930A>C