Canonical Allele Identifier: CA389620300
Gene: MGAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622022G>A , CM000676.2:g.49622022G>A GRCh38
NC_000014.8:g.50088740G>A , CM000676.1:g.50088740G>A GRCh37
NC_000014.7:g.49158490G>A NCBI36
NG_008920.1:g.6252G>A
NG_033054.1:g.3610C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.754G>A MANE Select ENSP00000307423.2:p.Ala252Thr
ENST00000305386.3:c.754G>A ENSP00000307423.2:p.Ala252Thr
NM_002408.3:c.754G>A NP_002399.1:p.Ala252Thr
NM_002408.4:c.754G>A MANE Select NP_002399.1:p.Ala252Thr