Canonical Allele Identifier: CA7172584
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs779133498
ExAC: 14:50088621 A / G
gnomAD v2: 14-50088621-A-G
gnomAD v4: 14-49621903-A-G
COSMIC: COSM4050978
MyVariant Identifiers: chr14:g.50088621A>G (hg19) chr14:g.49621903A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621903A>G , CM000676.2:g.49621903A>G GRCh38
NC_000014.8:g.50088621A>G , CM000676.1:g.50088621A>G GRCh37
NC_000014.7:g.49158371A>G NCBI36
NG_008920.1:g.6133A>G
NG_033054.1:g.3729T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.635A>G MANE Select ENSP00000307423.2:p.Asn212Ser
ENST00000305386.3:c.635A>G ENSP00000307423.2:p.Asn212Ser
NM_002408.3:c.635A>G NP_002399.1:p.Asn212Ser
NM_002408.4:c.635A>G MANE Select NP_002399.1:p.Asn212Ser
Search 100 bp 5'
Search 100 bp 3'