Canonical Allele Identifier: CA738208285
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1166615488
gnomAD v3: 1-68429754-A-C
gnomAD v4: 1-68429754-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429754A>C , CM000663.2:g.68429754A>C GRCh38
NC_000001.10:g.68895437A>C , CM000663.1:g.68895437A>C GRCh37
NC_000001.9:g.68668025A>C NCBI36
NG_008472.1:g.25206T>G
NG_008472.2:g.25206T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*22T>G MANE Select ENSP00000262340.5:n.*22T>G
ENST00000262340.5:c.*22T>G ENSP00000262340.5:n.*22T>G
NM_000329.2:c.*22T>G NP_000320.1:n.*22T>G
XM_017002027.1:c.*22T>G XP_016857516.1:n.*22T>G
NM_000329.3:c.*22T>G MANE Select NP_000320.1:n.*22T>G