Canonical Allele Identifier: CA486350247
Gene: MGAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50088853C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622135C>G , CM000676.2:g.49622135C>G GRCh38
NC_000014.8:g.50088853C>G , CM000676.1:g.50088853C>G GRCh37
NC_000014.7:g.49158603C>G NCBI36
NG_008920.1:g.6365C>G
NG_033054.1:g.3497G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.867C>G MANE Select ENSP00000307423.2:p.Leu289=
ENST00000305386.3:c.867C>G ENSP00000307423.2:p.Leu289=
NM_002408.3:c.867C>G NP_002399.1:p.Leu289=
NM_002408.4:c.867C>G MANE Select NP_002399.1:p.Leu289=
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