Canonical Allele Identifier: CA2135804783
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622036T= , CM000676.2:g.49622036T= GRCh38
NC_000014.8:g.50088754T= , CM000676.1:g.50088754T= GRCh37
NC_000014.7:g.49158504T= NCBI36
NG_008920.1:g.6266T=
NG_033054.1:g.3596A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.768T= MANE Select ENSP00000307423.2:p.Leu256=
ENST00000305386.3:c.768T= ENSP00000307423.2:p.Leu256=
NM_002408.3:c.768T= NP_002399.1:p.Leu256=
NM_002408.4:c.768T= MANE Select NP_002399.1:p.Leu256=