Canonical Allele Identifier: CA389620368
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1882870157

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622037T>C , CM000676.2:g.49622037T>C GRCh38
NC_000014.8:g.50088755T>C , CM000676.1:g.50088755T>C GRCh37
NC_000014.7:g.49158505T>C NCBI36
NG_008920.1:g.6267T>C
NG_033054.1:g.3595A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.769T>C MANE Select ENSP00000307423.2:p.Phe257Leu
ENST00000305386.3:c.769T>C ENSP00000307423.2:p.Phe257Leu
NM_002408.3:c.769T>C NP_002399.1:p.Phe257Leu
NM_002408.4:c.769T>C MANE Select NP_002399.1:p.Phe257Leu