Canonical Allele Identifier: CA2135804818
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622127G= , CM000676.2:g.49622127G= GRCh38
NC_000014.8:g.50088845G= , CM000676.1:g.50088845G= GRCh37
NC_000014.7:g.49158595G= NCBI36
NG_008920.1:g.6357G=
NG_033054.1:g.3505C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.859G= MANE Select ENSP00000307423.2:p.Asp287=
ENST00000305386.3:c.859G= ENSP00000307423.2:p.Asp287=
NM_002408.3:c.859G= NP_002399.1:p.Asp287=
NM_002408.4:c.859G= MANE Select NP_002399.1:p.Asp287=