Canonical Allele Identifier: CA2135804788
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622045A= , CM000676.2:g.49622045A= GRCh38
NC_000014.8:g.50088763A= , CM000676.1:g.50088763A= GRCh37
NC_000014.7:g.49158513A= NCBI36
NG_008920.1:g.6275A=
NG_033054.1:g.3587T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.777A= MANE Select ENSP00000307423.2:p.Glu259=
ENST00000305386.3:c.777A= ENSP00000307423.2:p.Glu259=
NM_002408.3:c.777A= NP_002399.1:p.Glu259=
NM_002408.4:c.777A= MANE Select NP_002399.1:p.Glu259=
Search 100 bp 5'
Search 100 bp 3'