Canonical Allele Identifier: CA406708631

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206338C>A (hg19) ; chr19:g.48703081C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703081C>A , CM000681.2:g.48703081C>A	GRCh38
NC_000019.9:g.49206338C>A , CM000681.1:g.49206338C>A	GRCh37
NC_000019.8:g.53898150C>A	NCBI36
NG_007511.1:g.12111C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.125C>A MANE Select	ENSP00000387498.2:p.Pro42Gln
ENST00000522966.2:c.125C>A	ENSP00000430227.2:p.Pro42Gln
ENST00000391876.5:c.125C>A	ENSP00000375748.4:p.Pro42Gln
ENST00000425340.2:c.125C>A	ENSP00000387498.2:p.Pro42Gln
ENST00000522966.1:c.125C>A	ENSP00000430227.1:p.Pro42Gln
NM_000511.5:c.125C>A	NP_000502.4:p.Pro42Gln
NM_001097638.2:c.125C>A	NP_001091107.1:p.Pro42Gln
NR_131188.1:n.768G>T
NM_000511.6:c.125C>A MANE Select	NP_000502.4:p.Pro42Gln
NM_001097638.3:c.125C>A	NP_001091107.1:p.Pro42Gln