Canonical Allele Identifier: CA486349878

Gene: MGAT2

Linked Data

• MyVariant Identifiers: chr14:g.50088394C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49621676C>T , CM000676.2:g.49621676C>T	GRCh38
NC_000014.8:g.50088394C>T , CM000676.1:g.50088394C>T	GRCh37
NC_000014.7:g.49158144C>T	NCBI36
NG_008920.1:g.5906C>T
NG_033054.1:g.3956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305386.4:c.408C>T MANE Select	ENSP00000307423.2:p.Asp136=
ENST00000305386.3:c.408C>T	ENSP00000307423.2:p.Asp136=
NM_002408.3:c.408C>T	NP_002399.1:p.Asp136=
NM_002408.4:c.408C>T MANE Select	NP_002399.1:p.Asp136=