Canonical Allele Identifier: CA389620348
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2139566766
MyVariant Identifiers: chr14:g.50088749A>G (hg19) chr14:g.49622031A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622031A>G , CM000676.2:g.49622031A>G GRCh38
NC_000014.8:g.50088749A>G , CM000676.1:g.50088749A>G GRCh37
NC_000014.7:g.49158499A>G NCBI36
NG_008920.1:g.6261A>G
NG_033054.1:g.3601T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.763A>G MANE Select ENSP00000307423.2:p.Ile255Val
ENST00000305386.3:c.763A>G ENSP00000307423.2:p.Ile255Val
NM_002408.3:c.763A>G NP_002399.1:p.Ile255Val
NM_002408.4:c.763A>G MANE Select NP_002399.1:p.Ile255Val
Search 100 bp 5'
Search 100 bp 3'