Canonical Allele Identifier: CA2135804831
Gene: MGAT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622156C= , CM000676.2:g.49622156C= GRCh38
NC_000014.8:g.50088874C= , CM000676.1:g.50088874C= GRCh37
NC_000014.7:g.49158624C= NCBI36
NG_008920.1:g.6386C=
NG_033054.1:g.3476G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.888C= MANE Select ENSP00000307423.2:p.Ala296=
ENST00000305386.3:c.888C= ENSP00000307423.2:p.Ala296=
NM_002408.3:c.888C= NP_002399.1:p.Ala296=
NM_002408.4:c.888C= MANE Select NP_002399.1:p.Ala296=
Search 100 bp 5'
Search 100 bp 3'