Canonical Allele Identifier: CA2135804529
Gene: MGAT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621697A= , CM000676.2:g.49621697A= GRCh38
NC_000014.8:g.50088415A= , CM000676.1:g.50088415A= GRCh37
NC_000014.7:g.49158165A= NCBI36
NG_008920.1:g.5927A=
NG_033054.1:g.3935T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.429A= MANE Select ENSP00000307423.2:p.Gly143=
ENST00000305386.3:c.429A= ENSP00000307423.2:p.Gly143=
NM_002408.3:c.429A= NP_002399.1:p.Gly143=
NM_002408.4:c.429A= MANE Select NP_002399.1:p.Gly143=
Search 100 bp 5'
Search 100 bp 3'