Canonical Allele Identifier: CA389619948
Gene: MGAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49621962C>A , CM000676.2:g.49621962C>A GRCh38
NC_000014.8:g.50088680C>A , CM000676.1:g.50088680C>A GRCh37
NC_000014.7:g.49158430C>A NCBI36
NG_008920.1:g.6192C>A
NG_033054.1:g.3670G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305386.4:c.694C>A MANE Select ENSP00000307423.2:p.His232Asn
ENST00000305386.3:c.694C>A ENSP00000307423.2:p.His232Asn
NM_002408.3:c.694C>A NP_002399.1:p.His232Asn
NM_002408.4:c.694C>A MANE Select NP_002399.1:p.His232Asn