Canonical Allele Identifier: CA2135804418
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621618A= , CM000676.2:g.49621618A= GRCh38
NC_000014.8:g.50088336A= , CM000676.1:g.50088336A= GRCh37
NC_000014.7:g.49158086A= NCBI36
NG_008920.1:g.5848A=
NG_033054.1:g.4014T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.350A= MANE Select ENSP00000307423.2:p.Glu117=
ENST00000305386.3:c.350A= ENSP00000307423.2:p.Glu117=
NM_002408.3:c.350A= NP_002399.1:p.Glu117=
NM_002408.4:c.350A= MANE Select NP_002399.1:p.Glu117=