Canonical Allele Identifier: CA2135804761
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621979G= , CM000676.2:g.49621979G= GRCh38
NC_000014.8:g.50088697G= , CM000676.1:g.50088697G= GRCh37
NC_000014.7:g.49158447G= NCBI36
NG_008920.1:g.6209G=
NG_033054.1:g.3653C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.711G= MANE Select ENSP00000307423.2:p.Lys237=
ENST00000305386.3:c.711G= ENSP00000307423.2:p.Lys237=
NM_002408.3:c.711G= NP_002399.1:p.Lys237=
NM_002408.4:c.711G= MANE Select NP_002399.1:p.Lys237=