Canonical Allele Identifier: CA902187
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1095670
ClinVar RCV Id: RCV001416651
dbSNP Id: rs372273815
gnomAD v2: 1-68896827-A-G
gnomAD v3: 1-68431144-A-G
gnomAD v4: 1-68431144-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431144A>G , CM000663.2:g.68431144A>G GRCh38
NC_000001.10:g.68896827A>G , CM000663.1:g.68896827A>G GRCh37
NC_000001.9:g.68669415A>G NCBI36
NG_008472.1:g.23816T>C
NG_008472.2:g.23816T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1371T>C MANE Select ENSP00000262340.5:p.Thr457=
ENST00000262340.5:c.1371T>C ENSP00000262340.5:p.Thr457=
NM_000329.2:c.1371T>C NP_000320.1:p.Thr457=
XM_017002027.1:c.1095T>C XP_016857516.1:p.Thr365=
NM_000329.3:c.1371T>C MANE Select NP_000320.1:p.Thr457=