Canonical Allele Identifier: CA406711379

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206842C>A (hg19) ; chr19:g.48703585C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703585C>A , CM000681.2:g.48703585C>A	GRCh38
NC_000019.9:g.49206842C>A , CM000681.1:g.49206842C>A	GRCh37
NC_000019.8:g.53898654C>A	NCBI36
NG_007511.1:g.12615C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.629C>A MANE Select	ENSP00000387498.2:p.Pro210Gln
ENST00000522966.2:c.629C>A	ENSP00000430227.2:p.Pro210Gln
ENST00000391876.5:c.629C>A	ENSP00000375748.4:p.Pro210Gln
ENST00000425340.2:c.629C>A	ENSP00000387498.2:p.Pro210Gln
ENST00000522966.1:c.629C>A	ENSP00000430227.1:p.Pro210Gln
NM_000511.5:c.629C>A	NP_000502.4:p.Pro210Gln
NM_001097638.2:c.629C>A	NP_001091107.1:p.Pro210Gln
NR_131188.1:n.264G>T
NM_000511.6:c.629C>A MANE Select	NP_000502.4:p.Pro210Gln
NM_001097638.3:c.629C>A	NP_001091107.1:p.Pro210Gln