Canonical Allele Identifier: CA389619936
Gene: MGAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621960A>G , CM000676.2:g.49621960A>G GRCh38
NC_000014.8:g.50088678A>G , CM000676.1:g.50088678A>G GRCh37
NC_000014.7:g.49158428A>G NCBI36
NG_008920.1:g.6190A>G
NG_033054.1:g.3672T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.692A>G MANE Select ENSP00000307423.2:p.Lys231Arg
ENST00000305386.3:c.692A>G ENSP00000307423.2:p.Lys231Arg
NM_002408.3:c.692A>G NP_002399.1:p.Lys231Arg
NM_002408.4:c.692A>G MANE Select NP_002399.1:p.Lys231Arg