Canonical Allele Identifier: CA902250
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1619194
ClinVar RCV Id: RCV002086551
dbSNP Id: rs373834001
gnomAD v2: 1-68897164-C-T
gnomAD v3: 1-68431481-C-T
gnomAD v4: 1-68431481-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431481C>T , CM000663.2:g.68431481C>T GRCh38
NC_000001.10:g.68897164C>T , CM000663.1:g.68897164C>T GRCh37
NC_000001.9:g.68669752C>T NCBI36
NG_008472.1:g.23479G>A
NG_008472.2:g.23479G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1233G>A MANE Select ENSP00000262340.5:p.Gly411=
ENST00000262340.5:c.1233G>A ENSP00000262340.5:p.Gly411=
NM_000329.2:c.1233G>A NP_000320.1:p.Gly411=
XM_017002027.1:c.957G>A XP_016857516.1:p.Gly319=
NM_000329.3:c.1233G>A MANE Select NP_000320.1:p.Gly411=