Canonical Allele Identifier: CA2832562019
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621613_49621614dup , CM000676.2:g.49621613_49621614dup GRCh38
NC_000014.8:g.50088331_50088332dup , CM000676.1:g.50088331_50088332dup GRCh37
NC_000014.7:g.49158081_49158082dup NCBI36
NG_008920.1:g.5843_5844dup
NG_033054.1:g.4022_4023dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.345_346dup MANE Select ENSP00000307423.2:p.Arg116ProfsTer?
ENST00000305386.3:c.345_346dup ENSP00000307423.2:p.Arg116ProfsTer?
NM_002408.3:c.345_346dup NP_002399.1:p.Arg116ProfsTer?
NM_002408.4:c.345_346dup MANE Select NP_002399.1:p.Arg116ProfsTer?