Canonical Allele Identifier: CA2135804491
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621675A= , CM000676.2:g.49621675A= GRCh38
NC_000014.8:g.50088393A= , CM000676.1:g.50088393A= GRCh37
NC_000014.7:g.49158143A= NCBI36
NG_008920.1:g.5905A=
NG_033054.1:g.3957T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.407A= MANE Select ENSP00000307423.2:p.Asp136=
ENST00000305386.3:c.407A= ENSP00000307423.2:p.Asp136=
NM_002408.3:c.407A= NP_002399.1:p.Asp136=
NM_002408.4:c.407A= MANE Select NP_002399.1:p.Asp136=
Search 100 bp 5'
Search 100 bp 3'