Canonical Allele Identifier: CA883026138

Gene: FUT2

Linked Data

• dbSNP Id: rs1170563891
• MyVariant Identifiers: chr19:g.49206737_49206738insGGA (hg19) ; chr19:g.48703480_48703481insGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703486_48703488dup , CM000681.2:g.48703486_48703488dup	GRCh38
NC_000019.9:g.49206743_49206745dup , CM000681.1:g.49206743_49206745dup	GRCh37
NC_000019.8:g.53898555_53898557dup	NCBI36
NG_007511.1:g.12516_12518dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000425340.3:c.530_532dup MANE Select	ENSP00000387498.2:p.Glu177_Ala178insGlu
ENST00000522966.2:c.530_532dup	ENSP00000430227.2:p.Glu177_Ala178insGlu
ENST00000391876.5:c.530_532dup	ENSP00000375748.4:p.Glu177_Ala178insGlu
ENST00000425340.2:c.530_532dup	ENSP00000387498.2:p.Glu177_Ala178insGlu
ENST00000522966.1:c.530_532dup	ENSP00000430227.1:p.Glu177_Ala178insGlu
NM_000511.5:c.530_532dup	NP_000502.4:p.Glu177_Ala178insGlu
NM_001097638.2:c.530_532dup	NP_001091107.1:p.Glu177_Ala178insGlu
NR_131188.1:n.366_368dup
NM_000511.6:c.530_532dup MANE Select	NP_000502.4:p.Glu177_Ala178insGlu
NM_001097638.3:c.530_532dup	NP_001091107.1:p.Glu177_Ala178insGlu