Canonical Allele Identifier: CA144141580

Gene: FUT9

Linked Data

• dbSNP Id: rs760554475
• gnomAD v4: 6-96212214-T-C
• MyVariant Identifiers: chr6:g.96660090T>C (hg19) ; chr6:g.96212214T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.96212214T>C , CM000668.2:g.96212214T>C	GRCh38
NC_000006.11:g.96660090T>C , CM000668.1:g.96660090T>C	GRCh37
NC_000006.10:g.96766811T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302103.6:c.*7979T>C MANE Select	ENSP00000302599.4:n.*7979T>C
ENST00000302103.5:c.*7979T>C	ENSP00000302599.4:n.*7979T>C
NM_006581.3:c.*7979T>C	NP_006572.2:n.*7979T>C
XR_942796.1:n.411-9199A>G
XR_942797.1:n.218-9199A>G
XR_942798.1:n.224-9199A>G
XR_942799.1:n.232-9199A>G
XR_942800.1:n.573-9199A>G
XM_011535383.2:c.*7979T>C	XP_011533685.1:n.*7979T>C
XM_011535385.2:c.*7979T>C	XP_011533687.1:n.*7979T>C
XM_017010188.1:c.*7979T>C	XP_016865677.1:n.*7979T>C
XM_017010190.1:c.*7979T>C	XP_016865679.1:n.*7979T>C
NM_006581.4:c.*7979T>C MANE Select	NP_006572.2:n.*7979T>C