Canonical Allele Identifier: CA2135804506
Gene: MGAT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621682T= , CM000676.2:g.49621682T= GRCh38
NC_000014.8:g.50088400T= , CM000676.1:g.50088400T= GRCh37
NC_000014.7:g.49158150T= NCBI36
NG_008920.1:g.5912T=
NG_033054.1:g.3950A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.414T= MANE Select ENSP00000307423.2:p.Leu138=
ENST00000305386.3:c.414T= ENSP00000307423.2:p.Leu138=
NM_002408.3:c.414T= NP_002399.1:p.Leu138=
NM_002408.4:c.414T= MANE Select NP_002399.1:p.Leu138=
Search 100 bp 5'
Search 100 bp 3'