Canonical Allele Identifier: CA260660703
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1012044822
MyVariant Identifiers: chr14:g.50088512T>G (hg19) chr14:g.49621794T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621794T>G , CM000676.2:g.49621794T>G GRCh38
NC_000014.8:g.50088512T>G , CM000676.1:g.50088512T>G GRCh37
NC_000014.7:g.49158262T>G NCBI36
NG_008920.1:g.6024T>G
NG_033054.1:g.3838A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.526T>G MANE Select ENSP00000307423.2:p.Phe176Val
ENST00000305386.3:c.526T>G ENSP00000307423.2:p.Phe176Val
NM_002408.3:c.526T>G NP_002399.1:p.Phe176Val
NM_002408.4:c.526T>G MANE Select NP_002399.1:p.Phe176Val
Search 100 bp 5'
Search 100 bp 3'