Canonical Allele Identifier: CA2135804613
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1882860833
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621767dup , CM000676.2:g.49621767dup GRCh38
NC_000014.8:g.50088485dup , CM000676.1:g.50088485dup GRCh37
NC_000014.7:g.49158235dup NCBI36
NG_008920.1:g.5997dup
NG_033054.1:g.3868dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.499dup MANE Select ENSP00000307423.2:p.Val167GlyfsTer20
ENST00000305386.3:c.499dup ENSP00000307423.2:p.Val167GlyfsTer20
NM_002408.3:c.499dup NP_002399.1:p.Val167GlyfsTer20
NM_002408.4:c.499dup MANE Select NP_002399.1:p.Val167GlyfsTer20
Search 100 bp 5'
Search 100 bp 3'