Canonical Allele Identifier: CA2624726681
Gene: MGAT2 HGNC NCBI

Linked Data

gnomAD v4: 14-49622044-AAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622047_49622048del , CM000676.2:g.49622047_49622048del GRCh38
NC_000014.8:g.50088765_50088766del , CM000676.1:g.50088765_50088766del GRCh37
NC_000014.7:g.49158515_49158516del NCBI36
NG_008920.1:g.6277_6278del
NG_033054.1:g.3586_3587del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.779_780del MANE Select ENSP00000307423.2:p.Glu260GlyfsTer25
ENST00000305386.3:c.779_780del ENSP00000307423.2:p.Glu260GlyfsTer25
NM_002408.3:c.779_780del NP_002399.1:p.Glu260GlyfsTer25
NM_002408.4:c.779_780del MANE Select NP_002399.1:p.Glu260GlyfsTer25
Search 100 bp 5'
Search 100 bp 3'