Canonical Allele Identifier: CA486350360
Gene: MGAT2 HGNC NCBI

Linked Data

gnomAD v4: 14-49621901-C-T
COSMIC: COSM1748857
MyVariant Identifiers: chr14:g.50088619C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621901C>T , CM000676.2:g.49621901C>T GRCh38
NC_000014.8:g.50088619C>T , CM000676.1:g.50088619C>T GRCh37
NC_000014.7:g.49158369C>T NCBI36
NG_008920.1:g.6131C>T
NG_033054.1:g.3731G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.633C>T MANE Select ENSP00000307423.2:p.Ile211=
ENST00000305386.3:c.633C>T ENSP00000307423.2:p.Ile211=
NM_002408.3:c.633C>T NP_002399.1:p.Ile211=
NM_002408.4:c.633C>T MANE Select NP_002399.1:p.Ile211=
Search 100 bp 5'
Search 100 bp 3'