Canonical Allele Identifier: CA2135804828
Gene: MGAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622149A= , CM000676.2:g.49622149A= GRCh38
NC_000014.8:g.50088867A= , CM000676.1:g.50088867A= GRCh37
NC_000014.7:g.49158617A= NCBI36
NG_008920.1:g.6379A=
NG_033054.1:g.3483T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.881A= MANE Select ENSP00000307423.2:p.Tyr294=
ENST00000305386.3:c.881A= ENSP00000307423.2:p.Tyr294=
NM_002408.3:c.881A= NP_002399.1:p.Tyr294=
NM_002408.4:c.881A= MANE Select NP_002399.1:p.Tyr294=
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