Canonical Allele Identifier: CA902507
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 716567
dbSNP Id: rs185049543
gnomAD v2: 1-68910268-T-C
gnomAD v3: 1-68444585-T-C
gnomAD v4: 1-68444585-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444585T>C , CM000663.2:g.68444585T>C GRCh38
NC_000001.10:g.68910268T>C , CM000663.1:g.68910268T>C GRCh37
NC_000001.9:g.68682856T>C NCBI36
NG_008472.1:g.10375A>G
NG_008472.2:g.10375A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.441A>G MANE Select ENSP00000262340.5:p.Thr147=
ENST00000262340.5:c.441A>G ENSP00000262340.5:p.Thr147=
NM_000329.2:c.441A>G NP_000320.1:p.Thr147=
XM_017002027.1:c.165A>G XP_016857516.1:p.Thr55=
NM_000329.3:c.441A>G MANE Select NP_000320.1:p.Thr147=