Canonical Allele Identifier: CA389620614
Gene: MGAT2 HGNC NCBI

Linked Data

gnomAD v4: 14-49622088-A-C
MyVariant Identifiers: chr14:g.50088806A>C (hg19) chr14:g.49622088A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622088A>C , CM000676.2:g.49622088A>C GRCh38
NC_000014.8:g.50088806A>C , CM000676.1:g.50088806A>C GRCh37
NC_000014.7:g.49158556A>C NCBI36
NG_008920.1:g.6318A>C
NG_033054.1:g.3544T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.820A>C MANE Select ENSP00000307423.2:p.Lys274Gln
ENST00000305386.3:c.820A>C ENSP00000307423.2:p.Lys274Gln
NM_002408.3:c.820A>C NP_002399.1:p.Lys274Gln
NM_002408.4:c.820A>C MANE Select NP_002399.1:p.Lys274Gln
Search 100 bp 5'
Search 100 bp 3'