Canonical Allele Identifier: CA486350004

Gene: MGAT2

Linked Data

• MyVariant Identifiers: chr14:g.50088928C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49622210C>G , CM000676.2:g.49622210C>G	GRCh38
NC_000014.8:g.50088928C>G , CM000676.1:g.50088928C>G	GRCh37
NC_000014.7:g.49158678C>G	NCBI36
NG_008920.1:g.6440C>G
NG_033054.1:g.3422G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305386.4:c.942C>G MANE Select	ENSP00000307423.2:p.Ser314=
ENST00000305386.3:c.942C>G	ENSP00000307423.2:p.Ser314=
NM_002408.3:c.942C>G	NP_002399.1:p.Ser314=
NM_002408.4:c.942C>G MANE Select	NP_002399.1:p.Ser314=