Canonical Allele Identifier: CA486349838
Gene: MGAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50088380A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621662A>C , CM000676.2:g.49621662A>C GRCh38
NC_000014.8:g.50088380A>C , CM000676.1:g.50088380A>C GRCh37
NC_000014.7:g.49158130A>C NCBI36
NG_008920.1:g.5892A>C
NG_033054.1:g.3970T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.394A>C MANE Select ENSP00000307423.2:p.Arg132=
ENST00000305386.3:c.394A>C ENSP00000307423.2:p.Arg132=
NM_002408.3:c.394A>C NP_002399.1:p.Arg132=
NM_002408.4:c.394A>C MANE Select NP_002399.1:p.Arg132=
Search 100 bp 5'
Search 100 bp 3'