Canonical Allele Identifier: CA9556296

Gene: FUT2

Linked Data

• dbSNP Id: rs768091739
• ExAC: 19:49206820 G / GGGGGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGT
• MyVariant Identifiers: chr19:g.49206820_49206821insGGGGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGT (hg19) ; chr19:g.48703563_48703564insGGGGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703566_48703567insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG , CM000681.2:g.48703566_48703567insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	GRCh38
NC_000019.9:g.49206823_49206824insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG , CM000681.1:g.49206823_49206824insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	GRCh37
NC_000019.8:g.53898635_53898636insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	NCBI36
NG_007511.1:g.12596_12597insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000425340.3:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG MANE Select	ENSP00000387498.2:p.Asp204GlyfsTer6
ENST00000522966.2:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	ENSP00000430227.2:p.Asp204GlyfsTer6
ENST00000391876.5:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	ENSP00000375748.4:p.Asp204GlyfsTer6
ENST00000425340.2:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	ENSP00000387498.2:p.Asp204GlyfsTer6
ENST00000522966.1:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	ENSP00000430227.1:p.Asp204GlyfsTer6
NM_000511.5:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	NP_000502.4:p.Asp204GlyfsTer6
NM_001097638.2:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	NP_001091107.1:p.Asp204GlyfsTer6
NR_131188.1:n.285_286insACCTTGGCCTCCCAAAGTGCTCAGATTATAGGCGTGAGCCACCCC
NM_000511.6:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG MANE Select	NP_000502.4:p.Asp204GlyfsTer6
NM_001097638.3:c.610_611insGTGGCTCACGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGG	NP_001091107.1:p.Asp204GlyfsTer6