Canonical Allele Identifier: CA2135804715
Gene: MGAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621865C= , CM000676.2:g.49621865C= GRCh38
NC_000014.8:g.50088583C= , CM000676.1:g.50088583C= GRCh37
NC_000014.7:g.49158333C= NCBI36
NG_008920.1:g.6095C=
NG_033054.1:g.3767G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.597C= MANE Select ENSP00000307423.2:p.Asp199=
ENST00000305386.3:c.597C= ENSP00000307423.2:p.Asp199=
NM_002408.3:c.597C= NP_002399.1:p.Asp199=
NM_002408.4:c.597C= MANE Select NP_002399.1:p.Asp199=