Canonical Allele Identifier: CA902240
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1205157
ClinVar RCV Id: RCV001571731
dbSNP Id: rs116540274
gnomAD v2: 1-68897125-C-T
gnomAD v3: 1-68431442-C-T
gnomAD v4: 1-68431442-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431442C>T , CM000663.2:g.68431442C>T GRCh38
NC_000001.10:g.68897125C>T , CM000663.1:g.68897125C>T GRCh37
NC_000001.9:g.68669713C>T NCBI36
NG_008472.1:g.23518G>A
NG_008472.2:g.23518G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+29G>A MANE Select ENSP00000262340.5:n.1243+29G>A
ENST00000262340.5:c.1243+29G>A ENSP00000262340.5:n.1243+29G>A
NM_000329.2:c.1243+29G>A NP_000320.1:n.1243+29G>A
XM_017002027.1:c.967+29G>A XP_016857516.1:n.967+29G>A
NM_000329.3:c.1243+29G>A MANE Select NP_000320.1:n.1243+29G>A