Canonical Allele Identifier: CA389619405
Gene: MGAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50088537A>C (hg19) chr14:g.49621819A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621819A>C , CM000676.2:g.49621819A>C GRCh38
NC_000014.8:g.50088537A>C , CM000676.1:g.50088537A>C GRCh37
NC_000014.7:g.49158287A>C NCBI36
NG_008920.1:g.6049A>C
NG_033054.1:g.3813T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.551A>C MANE Select ENSP00000307423.2:p.Tyr184Ser
ENST00000305386.3:c.551A>C ENSP00000307423.2:p.Tyr184Ser
NM_002408.3:c.551A>C NP_002399.1:p.Tyr184Ser
NM_002408.4:c.551A>C MANE Select NP_002399.1:p.Tyr184Ser
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Search 100 bp 3'