Canonical Allele Identifier: CA1002830245
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1379911395
gnomAD v3: 1-68430077-G-C
gnomAD v4: 1-68430077-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430077G>C , CM000663.2:g.68430077G>C GRCh38
NC_000001.10:g.68895760G>C , CM000663.1:g.68895760G>C GRCh37
NC_000001.9:g.68668348G>C NCBI36
NG_008472.1:g.24883C>G
NG_008472.2:g.24883C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-150C>G MANE Select ENSP00000262340.5:n.1451-150C>G
ENST00000262340.5:c.1451-150C>G ENSP00000262340.5:n.1451-150C>G
NM_000329.2:c.1451-150C>G NP_000320.1:n.1451-150C>G
XM_017002027.1:c.1175-150C>G XP_016857516.1:n.1175-150C>G
NM_000329.3:c.1451-150C>G MANE Select NP_000320.1:n.1451-150C>G