Canonical Allele Identifier: CA2650788638

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226896128-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226896128A>C , CM000663.2:g.226896128A>C	GRCh38
NC_000001.10:g.227083829A>C , CM000663.1:g.227083829A>C	GRCh37
NC_000001.9:g.225150452A>C	NCBI36
NG_007381.1:g.30557A>C
NG_012825.2:g.3593A>C
NG_007381.2:g.30945A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*549A>C	ENSP00000355741.2:n.*549A>C
ENST00000524196.6:c.*549A>C	ENSP00000429036.2:n.*549A>C
ENST00000676747.1:c.1189-1592A>C	ENSP00000503244.1:n.1189-1592A>C
ENST00000676884.1:c.*549A>C	ENSP00000503200.1:n.*549A>C
ENST00000676945.1:c.1191+2003A>C	ENSP00000504433.1:n.1191+2003A>C
ENST00000677599.1:c.1191+2003A>C	ENSP00000503673.1:n.1191+2003A>C
ENST00000678233.1:c.*8+541A>C	ENSP00000504728.1:n.*8+541A>C
ENST00000678655.1:c.1093-1592A>C	ENSP00000504230.1:n.1093-1592A>C
ENST00000678784.1:c.1073-1592A>C	ENSP00000504652.1:n.1073-1592A>C
ENST00000678820.1:c.1090-1592A>C	ENSP00000504138.1:n.1090-1592A>C
ENST00000678835.1:c.*757-1592A>C	ENSP00000504343.1:n.*757-1592A>C
ENST00000679098.1:c.*8+541A>C	ENSP00000504303.1:n.*8+541A>C
XR_001737316.2:n.1478-1592A>C
XR_001737317.2:n.1478-1592A>C