Canonical Allele Identifier: CA902207
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1124022
ClinVar RCV Id: RCV001455269
dbSNP Id: rs746506594
gnomAD v2: 1-68896968-A-G
gnomAD v3: 1-68431285-A-G
gnomAD v4: 1-68431285-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431285A>G , CM000663.2:g.68431285A>G GRCh38
NC_000001.10:g.68896968A>G , CM000663.1:g.68896968A>G GRCh37
NC_000001.9:g.68669556A>G NCBI36
NG_008472.1:g.23675T>C
NG_008472.2:g.23675T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1335T>C MANE Select ENSP00000262340.5:p.Asp445=
ENST00000262340.5:c.1335T>C ENSP00000262340.5:p.Asp445=
NM_000329.2:c.1335T>C NP_000320.1:p.Asp445=
XM_017002027.1:c.1059T>C XP_016857516.1:p.Asp353=
NM_000329.3:c.1335T>C MANE Select NP_000320.1:p.Asp445=