Canonical Allele Identifier: CA830107015

Gene: FUT9

Linked Data

• dbSNP Id: rs1337693371
• gnomAD v3: 6-96212252-G-A
• gnomAD v4: 6-96212252-G-A
• MyVariant Identifiers: chr6:g.96660128G>A (hg19) ; chr6:g.96212252G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.96212252G>A , CM000668.2:g.96212252G>A	GRCh38
NC_000006.11:g.96660128G>A , CM000668.1:g.96660128G>A	GRCh37
NC_000006.10:g.96766849G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302103.6:c.*8017G>A MANE Select	ENSP00000302599.4:n.*8017G>A
ENST00000302103.5:c.*8017G>A	ENSP00000302599.4:n.*8017G>A
NM_006581.3:c.*8017G>A	NP_006572.2:n.*8017G>A
XR_942796.1:n.411-9237C>T
XR_942797.1:n.218-9237C>T
XR_942798.1:n.224-9237C>T
XR_942799.1:n.232-9237C>T
XR_942800.1:n.573-9237C>T
XM_011535383.2:c.*8017G>A	XP_011533685.1:n.*8017G>A
XM_011535385.2:c.*8017G>A	XP_011533687.1:n.*8017G>A
XM_017010188.1:c.*8017G>A	XP_016865677.1:n.*8017G>A
XM_017010190.1:c.*8017G>A	XP_016865679.1:n.*8017G>A
NM_006581.4:c.*8017G>A MANE Select	NP_006572.2:n.*8017G>A