Canonical Allele Identifier: CA902241
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1588406
ClinVar RCV Id: RCV002117018
dbSNP Id: rs749922257
gnomAD v2: 1-68897136-T-C
gnomAD v4: 1-68431453-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431453T>C , CM000663.2:g.68431453T>C GRCh38
NC_000001.10:g.68897136T>C , CM000663.1:g.68897136T>C GRCh37
NC_000001.9:g.68669724T>C NCBI36
NG_008472.1:g.23507A>G
NG_008472.2:g.23507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+18A>G MANE Select ENSP00000262340.5:n.1243+18A>G
ENST00000262340.5:c.1243+18A>G ENSP00000262340.5:n.1243+18A>G
NM_000329.2:c.1243+18A>G NP_000320.1:n.1243+18A>G
XM_017002027.1:c.967+18A>G XP_016857516.1:n.967+18A>G
NM_000329.3:c.1243+18A>G MANE Select NP_000320.1:n.1243+18A>G