Canonical Allele Identifier: CA486349868
Gene: MGAT2 HGNC NCBI

Linked Data

gnomAD v4: 14-49621673-G-A
MyVariant Identifiers: chr14:g.50088391G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621673G>A , CM000676.2:g.49621673G>A GRCh38
NC_000014.8:g.50088391G>A , CM000676.1:g.50088391G>A GRCh37
NC_000014.7:g.49158141G>A NCBI36
NG_008920.1:g.5903G>A
NG_033054.1:g.3959C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.405G>A MANE Select ENSP00000307423.2:p.Leu135=
ENST00000305386.3:c.405G>A ENSP00000307423.2:p.Leu135=
NM_002408.3:c.405G>A NP_002399.1:p.Leu135=
NM_002408.4:c.405G>A MANE Select NP_002399.1:p.Leu135=
Search 100 bp 5'
Search 100 bp 3'