Canonical Allele Identifier: CA486350267
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1373489807
gnomAD v4: 14-49622144-G-A
MyVariant Identifiers: chr14:g.50088862G>A (hg19) chr14:g.49622144G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622144G>A , CM000676.2:g.49622144G>A GRCh38
NC_000014.8:g.50088862G>A , CM000676.1:g.50088862G>A GRCh37
NC_000014.7:g.49158612G>A NCBI36
NG_008920.1:g.6374G>A
NG_033054.1:g.3488C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.876G>A MANE Select ENSP00000307423.2:p.Gly292=
ENST00000305386.3:c.876G>A ENSP00000307423.2:p.Gly292=
NM_002408.3:c.876G>A NP_002399.1:p.Gly292=
NM_002408.4:c.876G>A MANE Select NP_002399.1:p.Gly292=
Search 100 bp 5'
Search 100 bp 3'