Canonical Allele Identifier: CA23562298
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs543498979
gnomAD v2: 1-68895342-G-A
gnomAD v3: 1-68429659-G-A
gnomAD v4: 1-68429659-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429659G>A , CM000663.2:g.68429659G>A GRCh38
NC_000001.10:g.68895342G>A , CM000663.1:g.68895342G>A GRCh37
NC_000001.9:g.68667930G>A NCBI36
NG_008472.1:g.25301C>T
NG_008472.2:g.25301C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*117C>T MANE Select ENSP00000262340.5:n.*117C>T
ENST00000262340.5:c.*117C>T ENSP00000262340.5:n.*117C>T
NM_000329.2:c.*117C>T NP_000320.1:n.*117C>T
XM_017002027.1:c.*117C>T XP_016857516.1:n.*117C>T
NM_000329.3:c.*117C>T MANE Select NP_000320.1:n.*117C>T