Canonical Allele Identifier: CA226551
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 98869
dbSNP Id: rs56021047
gnomAD v2: 1-68910277-G-A
gnomAD v3: 1-68444594-G-A
gnomAD v4: 1-68444594-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444594G>A , CM000663.2:g.68444594G>A GRCh38
NC_000001.10:g.68910277G>A , CM000663.1:g.68910277G>A GRCh37
NC_000001.9:g.68682865G>A NCBI36
NG_008472.1:g.10366C>T
NG_008472.2:g.10366C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.432C>T MANE Select ENSP00000262340.5:p.Tyr144=
ENST00000262340.5:c.432C>T ENSP00000262340.5:p.Tyr144=
NM_000329.2:c.432C>T NP_000320.1:p.Tyr144=
XM_017002027.1:c.156C>T XP_016857516.1:p.Tyr52=
NM_000329.3:c.432C>T MANE Select NP_000320.1:p.Tyr144=