Canonical Allele Identifier: CA2624726685
Gene: MGAT2 HGNC NCBI

Linked Data

gnomAD v4: 14-49622096-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622099del , CM000676.2:g.49622099del GRCh38
NC_000014.8:g.50088817del , CM000676.1:g.50088817del GRCh37
NC_000014.7:g.49158567del NCBI36
NG_008920.1:g.6329del
NG_033054.1:g.3535del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.831del MANE Select ENSP00000307423.2:p.Lys277AsnfsTer2
ENST00000305386.3:c.831del ENSP00000307423.2:p.Lys277AsnfsTer2
NM_002408.3:c.831del NP_002399.1:p.Lys277AsnfsTer2
NM_002408.4:c.831del MANE Select NP_002399.1:p.Lys277AsnfsTer2
Search 100 bp 5'
Search 100 bp 3'