Canonical Allele Identifier: CA1648673479
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1562168877

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212201C>G , CM000668.2:g.96212201C>G GRCh38
NC_000006.11:g.96660077C>G , CM000668.1:g.96660077C>G GRCh37
NC_000006.10:g.96766798C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.*7966C>G MANE Select ENSP00000302599.4:n.*7966C>G
ENST00000302103.5:c.*7966C>G ENSP00000302599.4:n.*7966C>G
NM_006581.3:c.*7966C>G NP_006572.2:n.*7966C>G
XR_942796.1:n.411-9186G>C
XR_942797.1:n.218-9186G>C
XR_942798.1:n.224-9186G>C
XR_942799.1:n.232-9186G>C
XR_942800.1:n.573-9186G>C
XM_011535383.2:c.*7966C>G XP_011533685.1:n.*7966C>G
XM_011535385.2:c.*7966C>G XP_011533687.1:n.*7966C>G
XM_017010188.1:c.*7966C>G XP_016865677.1:n.*7966C>G
XM_017010190.1:c.*7966C>G XP_016865679.1:n.*7966C>G
NM_006581.4:c.*7966C>G MANE Select NP_006572.2:n.*7966C>G