Canonical Allele Identifier: CA389619716
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1882866324

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621918A>T , CM000676.2:g.49621918A>T GRCh38
NC_000014.8:g.50088636A>T , CM000676.1:g.50088636A>T GRCh37
NC_000014.7:g.49158386A>T NCBI36
NG_008920.1:g.6148A>T
NG_033054.1:g.3714T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.650A>T MANE Select ENSP00000307423.2:p.Asp217Val
ENST00000305386.3:c.650A>T ENSP00000307423.2:p.Asp217Val
NM_002408.3:c.650A>T NP_002399.1:p.Asp217Val
NM_002408.4:c.650A>T MANE Select NP_002399.1:p.Asp217Val