Canonical Allele Identifier: CA2135804771
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622003G= , CM000676.2:g.49622003G= GRCh38
NC_000014.8:g.50088721G= , CM000676.1:g.50088721G= GRCh37
NC_000014.7:g.49158471G= NCBI36
NG_008920.1:g.6233G=
NG_033054.1:g.3629C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.735G= MANE Select ENSP00000307423.2:p.Val245=
ENST00000305386.3:c.735G= ENSP00000307423.2:p.Val245=
NM_002408.3:c.735G= NP_002399.1:p.Val245=
NM_002408.4:c.735G= MANE Select NP_002399.1:p.Val245=
Search 100 bp 5'
Search 100 bp 3'