Canonical Allele Identifier: CA389619601

Gene: MGAT2

Linked Data

• MyVariant Identifiers: chr14:g.50088614T>G (hg19) ; chr14:g.49621896T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49621896T>G , CM000676.2:g.49621896T>G	GRCh38
NC_000014.8:g.50088614T>G , CM000676.1:g.50088614T>G	GRCh37
NC_000014.7:g.49158364T>G	NCBI36
NG_008920.1:g.6126T>G
NG_033054.1:g.3736A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305386.4:c.628T>G MANE Select	ENSP00000307423.2:p.Cys210Gly
ENST00000305386.3:c.628T>G	ENSP00000307423.2:p.Cys210Gly
NM_002408.3:c.628T>G	NP_002399.1:p.Cys210Gly
NM_002408.4:c.628T>G MANE Select	NP_002399.1:p.Cys210Gly