Canonical Allele Identifier: CA2624726683
Gene: MGAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622091_49622093dup , CM000676.2:g.49622091_49622093dup GRCh38
NC_000014.8:g.50088809_50088811dup , CM000676.1:g.50088809_50088811dup GRCh37
NC_000014.7:g.49158559_49158561dup NCBI36
NG_008920.1:g.6321_6323dup
NG_033054.1:g.3540_3542dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.823_825dup MANE Select ENSP00000307423.2:p.Met275_Trp276insMet
ENST00000305386.3:c.823_825dup ENSP00000307423.2:p.Met275_Trp276insMet
NM_002408.3:c.823_825dup NP_002399.1:p.Met275_Trp276insMet
NM_002408.4:c.823_825dup MANE Select NP_002399.1:p.Met275_Trp276insMet