Canonical Allele Identifier: CA2135804594
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1882859942
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621750_49621753del , CM000676.2:g.49621750_49621753del GRCh38
NC_000014.8:g.50088468_50088471del , CM000676.1:g.50088468_50088471del GRCh37
NC_000014.7:g.49158218_49158221del NCBI36
NG_008920.1:g.5980_5983del
NG_033054.1:g.3883_3886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.482_485del MANE Select ENSP00000307423.2:p.Asn161SerfsTer2
ENST00000305386.3:c.482_485del ENSP00000307423.2:p.Asn161SerfsTer2
NM_002408.3:c.482_485del NP_002399.1:p.Asn161SerfsTer2
NM_002408.4:c.482_485del MANE Select NP_002399.1:p.Asn161SerfsTer2
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