Canonical Allele Identifier: CA902188
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517547
ClinVar RCV Id: RCV002027434
dbSNP Id: rs755805126
gnomAD v2: 1-68896832-C-G
gnomAD v3: 1-68431149-C-G
gnomAD v4: 1-68431149-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431149C>G , CM000663.2:g.68431149C>G GRCh38
NC_000001.10:g.68896832C>G , CM000663.1:g.68896832C>G GRCh37
NC_000001.9:g.68669420C>G NCBI36
NG_008472.1:g.23811G>C
NG_008472.2:g.23811G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1366G>C MANE Select ENSP00000262340.5:p.Glu456Gln
ENST00000262340.5:c.1366G>C ENSP00000262340.5:p.Glu456Gln
NM_000329.2:c.1366G>C NP_000320.1:p.Glu456Gln
XM_017002027.1:c.1090G>C XP_016857516.1:p.Glu364Gln
NM_000329.3:c.1366G>C MANE Select NP_000320.1:p.Glu456Gln