Canonical Allele Identifier: CA389618958
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1333061086

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621696G>T , CM000676.2:g.49621696G>T GRCh38
NC_000014.8:g.50088414G>T , CM000676.1:g.50088414G>T GRCh37
NC_000014.7:g.49158164G>T NCBI36
NG_008920.1:g.5926G>T
NG_033054.1:g.3936C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.428G>T MANE Select ENSP00000307423.2:p.Gly143Val
ENST00000305386.3:c.428G>T ENSP00000307423.2:p.Gly143Val
NM_002408.3:c.428G>T NP_002399.1:p.Gly143Val
NM_002408.4:c.428G>T MANE Select NP_002399.1:p.Gly143Val