Canonical Allele Identifier: CA260660676
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs762127794
gnomAD v2: 14-50088453-G-T
gnomAD v4: 14-49621735-G-T
MyVariant Identifiers: chr14:g.50088453G>T (hg19) chr14:g.49621735G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621735G>T , CM000676.2:g.49621735G>T GRCh38
NC_000014.8:g.50088453G>T , CM000676.1:g.50088453G>T GRCh37
NC_000014.7:g.49158203G>T NCBI36
NG_008920.1:g.5965G>T
NG_033054.1:g.3897C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.467G>T MANE Select ENSP00000307423.2:p.Trp156Leu
ENST00000305386.3:c.467G>T ENSP00000307423.2:p.Trp156Leu
NM_002408.3:c.467G>T NP_002399.1:p.Trp156Leu
NM_002408.4:c.467G>T MANE Select NP_002399.1:p.Trp156Leu
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Search 100 bp 3'