Canonical Allele Identifier: CA486349908
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1397221233
gnomAD v2: 14-50088406-A-G
gnomAD v4: 14-49621688-A-G
MyVariant Identifiers: chr14:g.50088406A>G (hg19) chr14:g.49621688A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621688A>G , CM000676.2:g.49621688A>G GRCh38
NC_000014.8:g.50088406A>G , CM000676.1:g.50088406A>G GRCh37
NC_000014.7:g.49158156A>G NCBI36
NG_008920.1:g.5918A>G
NG_033054.1:g.3944T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.420A>G MANE Select ENSP00000307423.2:p.Lys140=
ENST00000305386.3:c.420A>G ENSP00000307423.2:p.Lys140=
NM_002408.3:c.420A>G NP_002399.1:p.Lys140=
NM_002408.4:c.420A>G MANE Select NP_002399.1:p.Lys140=
Search 100 bp 5'
Search 100 bp 3'