Canonical Allele Identifier: CA389620144
Gene: MGAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1882868613

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621992T>G , CM000676.2:g.49621992T>G GRCh38
NC_000014.8:g.50088710T>G , CM000676.1:g.50088710T>G GRCh37
NC_000014.7:g.49158460T>G NCBI36
NG_008920.1:g.6222T>G
NG_033054.1:g.3640A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305386.4:c.724T>G MANE Select ENSP00000307423.2:p.Trp242Gly
ENST00000305386.3:c.724T>G ENSP00000307423.2:p.Trp242Gly
NM_002408.3:c.724T>G NP_002399.1:p.Trp242Gly
NM_002408.4:c.724T>G MANE Select NP_002399.1:p.Trp242Gly