Canonical Allele Identifier: CA902196
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1255052
ClinVar RCV Id: RCV001659235
dbSNP Id: rs13375676
gnomAD v2: 1-68896898-A-G
gnomAD v3: 1-68431215-A-G
gnomAD v4: 1-68431215-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431215A>G , CM000663.2:g.68431215A>G GRCh38
NC_000001.10:g.68896898A>G , CM000663.1:g.68896898A>G GRCh37
NC_000001.9:g.68669486A>G NCBI36
NG_008472.1:g.23745T>C
NG_008472.2:g.23745T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1339-39T>C MANE Select ENSP00000262340.5:n.1339-39T>C
ENST00000262340.5:c.1339-39T>C ENSP00000262340.5:n.1339-39T>C
NM_000329.2:c.1339-39T>C NP_000320.1:n.1339-39T>C
XM_017002027.1:c.1063-39T>C XP_016857516.1:n.1063-39T>C
NM_000329.3:c.1339-39T>C MANE Select NP_000320.1:n.1339-39T>C