Canonical Allele Identifier: CA389620941
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1227641577

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622167T>A , CM000676.2:g.49622167T>A GRCh38
NC_000014.8:g.50088885T>A , CM000676.1:g.50088885T>A GRCh37
NC_000014.7:g.49158635T>A NCBI36
NG_008920.1:g.6397T>A
NG_033054.1:g.3465A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.899T>A MANE Select ENSP00000307423.2:p.Phe300Tyr
ENST00000305386.3:c.899T>A ENSP00000307423.2:p.Phe300Tyr
NM_002408.3:c.899T>A NP_002399.1:p.Phe300Tyr
NM_002408.4:c.899T>A MANE Select NP_002399.1:p.Phe300Tyr