Canonical Allele Identifier: CA902338
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1151727
ClinVar RCV Id: RCV001492791
dbSNP Id: rs753954638
gnomAD v2: 1-68904666-T-C
gnomAD v3: 1-68438983-T-C
gnomAD v4: 1-68438983-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438983T>C , CM000663.2:g.68438983T>C GRCh38
NC_000001.10:g.68904666T>C , CM000663.1:g.68904666T>C GRCh37
NC_000001.9:g.68677254T>C NCBI36
NG_008472.1:g.15977A>G
NG_008472.2:g.15977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.957A>G MANE Select ENSP00000262340.5:p.Glu319=
ENST00000262340.5:c.957A>G ENSP00000262340.5:p.Glu319=
NM_000329.2:c.957A>G NP_000320.1:p.Glu319=
XM_017002027.1:c.681A>G XP_016857516.1:p.Glu227=
NM_000329.3:c.957A>G MANE Select NP_000320.1:p.Glu319=