Canonical Allele Identifier: CA144124233
Gene: FUT9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10499003

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057343A>C , CM000668.2:g.96057343A>C GRCh38
NC_000006.11:g.96505219A>C , CM000668.1:g.96505219A>C GRCh37
NC_000006.10:g.96611940A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_006581.3:c.-98+41131A>C VV NP_006572.2:p.=
XM_011535384.1:c.-98+36370A>C XP_011533686.1:p.=
XM_017010190.1:c.-215+41131A>C XP_016865679.1:p.=
XR_001744267.2:n.1915T>G
NM_006581.4:c.-98+41131A>C VV MANE Preferred
ENST00000302103.5:c.-98+41131A>C ENSP00000302599.4:p.=