Canonical Allele Identifier: CA486350163
Gene: MGAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50088520T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621802T>A , CM000676.2:g.49621802T>A GRCh38
NC_000014.8:g.50088520T>A , CM000676.1:g.50088520T>A GRCh37
NC_000014.7:g.49158270T>A NCBI36
NG_008920.1:g.6032T>A
NG_033054.1:g.3830A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.534T>A MANE Select ENSP00000307423.2:p.Pro178=
ENST00000305386.3:c.534T>A ENSP00000307423.2:p.Pro178=
NM_002408.3:c.534T>A NP_002399.1:p.Pro178=
NM_002408.4:c.534T>A MANE Select NP_002399.1:p.Pro178=
Search 100 bp 5'
Search 100 bp 3'