Canonical Allele Identifier: CA23564245
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1565282
ClinVar RCV Id: RCV002205233
dbSNP Id: rs375375768
gnomAD v2: 1-68897145-T-A
gnomAD v4: 1-68431462-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431462T>A , CM000663.2:g.68431462T>A GRCh38
NC_000001.10:g.68897145T>A , CM000663.1:g.68897145T>A GRCh37
NC_000001.9:g.68669733T>A NCBI36
NG_008472.1:g.23498A>T
NG_008472.2:g.23498A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+9A>T MANE Select ENSP00000262340.5:n.1243+9A>T
ENST00000262340.5:c.1243+9A>T ENSP00000262340.5:n.1243+9A>T
NM_000329.2:c.1243+9A>T NP_000320.1:n.1243+9A>T
XM_017002027.1:c.967+9A>T XP_016857516.1:n.967+9A>T
NM_000329.3:c.1243+9A>T MANE Select NP_000320.1:n.1243+9A>T