Canonical Allele Identifier: CA389619518
Gene: MGAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50088587C>G (hg19) chr14:g.49621869C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621869C>G , CM000676.2:g.49621869C>G GRCh38
NC_000014.8:g.50088587C>G , CM000676.1:g.50088587C>G GRCh37
NC_000014.7:g.49158337C>G NCBI36
NG_008920.1:g.6099C>G
NG_033054.1:g.3763G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.601C>G MANE Select ENSP00000307423.2:p.Pro201Ala
ENST00000305386.3:c.601C>G ENSP00000307423.2:p.Pro201Ala
NM_002408.3:c.601C>G NP_002399.1:p.Pro201Ala
NM_002408.4:c.601C>G MANE Select NP_002399.1:p.Pro201Ala
Search 100 bp 5'
Search 100 bp 3'