Canonical Allele Identifier: CA732340279
Gene: PSEN2 HGNC NCBI

Linked Data

dbSNP Id: rs1423360113

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226870485C>T , CM000663.2:g.226870485C>T GRCh38
NC_000001.10:g.227058186C>T , CM000663.1:g.227058186C>T GRCh37
NC_000001.9:g.225124809C>T NCBI36
NG_007381.1:g.4914C>T
NG_007381.2:g.5302C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.-370C>T ENSP00000355741.2:n.-370C>T
ENST00000524196.6:c.-370C>T ENSP00000429036.2:n.-370C>T
ENST00000676884.1:c.-370C>T ENSP00000503200.1:n.-370C>T
ENST00000676888.1:c.-370C>T ENSP00000504483.1:n.-370C>T
ENST00000524196.5:c.-370C>T ENSP00000429036.1:n.-370C>T
XR_949226.1:n.35G>A