Canonical Allele Identifier: CA389619013
Gene: MGAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621708T>G , CM000676.2:g.49621708T>G GRCh38
NC_000014.8:g.50088426T>G , CM000676.1:g.50088426T>G GRCh37
NC_000014.7:g.49158176T>G NCBI36
NG_008920.1:g.5938T>G
NG_033054.1:g.3924A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.440T>G MANE Select ENSP00000307423.2:p.Val147Gly
ENST00000305386.3:c.440T>G ENSP00000307423.2:p.Val147Gly
NM_002408.3:c.440T>G NP_002399.1:p.Val147Gly
NM_002408.4:c.440T>G MANE Select NP_002399.1:p.Val147Gly