Canonical Allele Identifier: CA144124233
Gene: FUT9 HGNC NCBI
dbSNP:
10499003
gnomAD v2:
6:96505219 A / C
gnomAD v3:
6:96057343 A / C
gnomAD v4:
chr6-96057343-A-C
Joint Max Group AF 0.16488217 (NFE)
Genomes Max Group AF 0.16488217 (NFE)
MyVariant.info:
GRCh38 chr6:g.96057343A>C
GRCh37 chr6:g.96505219A>C
JSON-LD

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
ENST00000302103.6:c.-98+41131A>C MANE Select ENSP00000302599.4:n.-98+41131A>C
ENST00000302103.5:c.-98+41131A>C ENSP00000302599.4:n.-98+41131A>C
NM_006581.3:c.-98+41131A>C NP_006572.2:n.-98+41131A>C
XM_011535384.1:c.-98+36370A>C XP_011533686.1:n.-98+36370A>C
XM_017010190.1:c.-215+41131A>C XP_016865679.1:n.-215+41131A>C
XR_001744267.2:n.1915T>G
NM_006581.4:c.-98+41131A>C MANE Select NP_006572.2:n.-98+41131A>C
Search 100 bp 5'
Search 100 bp 3'