Canonical Allele Identifier: CA902118
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs763820730
gnomAD v2: 1-68895428-G-T
gnomAD v4: 1-68429745-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429745G>T , CM000663.2:g.68429745G>T GRCh38
NC_000001.10:g.68895428G>T , CM000663.1:g.68895428G>T GRCh37
NC_000001.9:g.68668016G>T NCBI36
NG_008472.1:g.25215C>A
NG_008472.2:g.25215C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*31C>A MANE Select ENSP00000262340.5:n.*31C>A
ENST00000262340.5:c.*31C>A ENSP00000262340.5:n.*31C>A
NM_000329.2:c.*31C>A NP_000320.1:n.*31C>A
XM_017002027.1:c.*31C>A XP_016857516.1:n.*31C>A
NM_000329.3:c.*31C>A MANE Select NP_000320.1:n.*31C>A