Canonical Allele Identifier: CA486350258
Gene: MGAT2 HGNC NCBI

Linked Data

gnomAD v4: 14-49621634-C-A
MyVariant Identifiers: chr14:g.50088352C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621634C>A , CM000676.2:g.49621634C>A GRCh38
NC_000014.8:g.50088352C>A , CM000676.1:g.50088352C>A GRCh37
NC_000014.7:g.49158102C>A NCBI36
NG_008920.1:g.5864C>A
NG_033054.1:g.3998G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.366C>A MANE Select ENSP00000307423.2:p.Val122=
ENST00000305386.3:c.366C>A ENSP00000307423.2:p.Val122=
NM_002408.3:c.366C>A NP_002399.1:p.Val122=
NM_002408.4:c.366C>A MANE Select NP_002399.1:p.Val122=
Search 100 bp 5'
Search 100 bp 3'