Canonical Allele Identifier: CA340742364
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1430518
ClinVar RCV Id: RCV001931517
dbSNP Id: rs1645824155
gnomAD v3: 1-68431286-T-C
gnomAD v4: 1-68431286-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431286T>C , CM000663.2:g.68431286T>C GRCh38
NC_000001.10:g.68896969T>C , CM000663.1:g.68896969T>C GRCh37
NC_000001.9:g.68669557T>C NCBI36
NG_008472.1:g.23674A>G
NG_008472.2:g.23674A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1334A>G MANE Select ENSP00000262340.5:p.Asp445Gly
ENST00000262340.5:c.1334A>G ENSP00000262340.5:p.Asp445Gly
NM_000329.2:c.1334A>G NP_000320.1:p.Asp445Gly
XM_017002027.1:c.1058A>G XP_016857516.1:p.Asp353Gly
NM_000329.3:c.1334A>G MANE Select NP_000320.1:p.Asp445Gly