Canonical Allele Identifier: CA486350235
Gene: MGAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50088556T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621838T>A , CM000676.2:g.49621838T>A GRCh38
NC_000014.8:g.50088556T>A , CM000676.1:g.50088556T>A GRCh37
NC_000014.7:g.49158306T>A NCBI36
NG_008920.1:g.6068T>A
NG_033054.1:g.3794A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.570T>A MANE Select ENSP00000307423.2:p.Gly190=
ENST00000305386.3:c.570T>A ENSP00000307423.2:p.Gly190=
NM_002408.3:c.570T>A NP_002399.1:p.Gly190=
NM_002408.4:c.570T>A MANE Select NP_002399.1:p.Gly190=
Search 100 bp 5'
Search 100 bp 3'