Canonical Allele Identifier: CA2135804835
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622167T= , CM000676.2:g.49622167T= GRCh38
NC_000014.8:g.50088885T= , CM000676.1:g.50088885T= GRCh37
NC_000014.7:g.49158635T= NCBI36
NG_008920.1:g.6397T=
NG_033054.1:g.3465A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.899T= MANE Select ENSP00000307423.2:p.Phe300=
ENST00000305386.3:c.899T= ENSP00000307423.2:p.Phe300=
NM_002408.3:c.899T= NP_002399.1:p.Phe300=
NM_002408.4:c.899T= MANE Select NP_002399.1:p.Phe300=
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