Canonical Allele Identifier: CA2135804816

Gene: MGAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.49622120T= , CM000676.2:g.49622120T=	GRCh38
NC_000014.8:g.50088838T= , CM000676.1:g.50088838T=	GRCh37
NC_000014.7:g.49158588T=	NCBI36
NG_008920.1:g.6350T=
NG_033054.1:g.3512A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305386.4:c.852T= MANE Select	ENSP00000307423.2:p.Pro284=
ENST00000305386.3:c.852T=	ENSP00000307423.2:p.Pro284=
NM_002408.3:c.852T=	NP_002399.1:p.Pro284=
NM_002408.4:c.852T= MANE Select	NP_002399.1:p.Pro284=