Canonical Allele Identifier: CA406709282

Gene: FUT2

Linked Data

• MyVariant Identifiers: chr19:g.49206487C>G (hg19) ; chr19:g.48703230C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48703230C>G , CM000681.2:g.48703230C>G	GRCh38
NC_000019.9:g.49206487C>G , CM000681.1:g.49206487C>G	GRCh37
NC_000019.8:g.53898299C>G	NCBI36
NG_007511.1:g.12260C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425340.3:c.274C>G MANE Select	ENSP00000387498.2:p.Pro92Ala
ENST00000522966.2:c.274C>G	ENSP00000430227.2:p.Pro92Ala
ENST00000391876.5:c.274C>G	ENSP00000375748.4:p.Pro92Ala
ENST00000425340.2:c.274C>G	ENSP00000387498.2:p.Pro92Ala
ENST00000522966.1:c.274C>G	ENSP00000430227.1:p.Pro92Ala
NM_000511.5:c.274C>G	NP_000502.4:p.Pro92Ala
NM_001097638.2:c.274C>G	NP_001091107.1:p.Pro92Ala
NR_131188.1:n.619G>C
NM_000511.6:c.274C>G MANE Select	NP_000502.4:p.Pro92Ala
NM_001097638.3:c.274C>G	NP_001091107.1:p.Pro92Ala