Canonical Allele Identifier: CA406711357
Gene: FUT2 HGNC NCBI

Linked Data

dbSNP Id: rs1200539933

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703582T>A , CM000681.2:g.48703582T>A GRCh38
NC_000019.9:g.49206839T>A , CM000681.1:g.49206839T>A GRCh37
NC_000019.8:g.53898651T>A NCBI36
NG_007511.1:g.12612T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.626T>A MANE Select ENSP00000387498.2:p.Met209Lys
ENST00000522966.2:c.626T>A ENSP00000430227.2:p.Met209Lys
ENST00000391876.5:c.626T>A ENSP00000375748.4:p.Met209Lys
ENST00000425340.2:c.626T>A ENSP00000387498.2:p.Met209Lys
ENST00000522966.1:c.626T>A ENSP00000430227.1:p.Met209Lys
NM_000511.5:c.626T>A NP_000502.4:p.Met209Lys
NM_001097638.2:c.626T>A NP_001091107.1:p.Met209Lys
NR_131188.1:n.267A>T
NM_000511.6:c.626T>A MANE Select NP_000502.4:p.Met209Lys
NM_001097638.3:c.626T>A NP_001091107.1:p.Met209Lys