Canonical Allele Identifier: CA738208269
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs915277974

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429712G>C , CM000663.2:g.68429712G>C GRCh38
NC_000001.10:g.68895395G>C , CM000663.1:g.68895395G>C GRCh37
NC_000001.9:g.68667983G>C NCBI36
NG_008472.1:g.25248C>G
NG_008472.2:g.25248C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*64C>G MANE Select ENSP00000262340.5:n.*64C>G
ENST00000262340.5:c.*64C>G ENSP00000262340.5:n.*64C>G
NM_000329.2:c.*64C>G NP_000320.1:n.*64C>G
XM_017002027.1:c.*64C>G XP_016857516.1:n.*64C>G
NM_000329.3:c.*64C>G MANE Select NP_000320.1:n.*64C>G