Canonical Allele Identifier: CA902236
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs762775279
gnomAD v2: 1-68897108-A-C
gnomAD v3: 1-68431425-A-C
gnomAD v4: 1-68431425-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431425A>C , CM000663.2:g.68431425A>C GRCh38
NC_000001.10:g.68897108A>C , CM000663.1:g.68897108A>C GRCh37
NC_000001.9:g.68669696A>C NCBI36
NG_008472.1:g.23535T>G
NG_008472.2:g.23535T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+46T>G MANE Select ENSP00000262340.5:n.1243+46T>G
ENST00000262340.5:c.1243+46T>G ENSP00000262340.5:n.1243+46T>G
NM_000329.2:c.1243+46T>G NP_000320.1:n.1243+46T>G
XM_017002027.1:c.967+46T>G XP_016857516.1:n.967+46T>G
NM_000329.3:c.1243+46T>G MANE Select NP_000320.1:n.1243+46T>G