Canonical Allele Identifier: CA2530660219
Gene: MGAT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621758_49621764dup , CM000676.2:g.49621758_49621764dup GRCh38
NC_000014.8:g.50088476_50088482dup , CM000676.1:g.50088476_50088482dup GRCh37
NC_000014.7:g.49158226_49158232dup NCBI36
NG_008920.1:g.5988_5994dup
NG_033054.1:g.3869_3875dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.490_496dup MANE Select ENSP00000307423.2:p.Gly166AspfsTer23
ENST00000305386.3:c.490_496dup ENSP00000307423.2:p.Gly166AspfsTer23
NM_002408.3:c.490_496dup NP_002399.1:p.Gly166AspfsTer23
NM_002408.4:c.490_496dup MANE Select NP_002399.1:p.Gly166AspfsTer23
Search 100 bp 5'
Search 100 bp 3'