Canonical Allele Identifier: CA1173557969
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1645823823
gnomAD v4: 1-68431237-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431237T>G , CM000663.2:g.68431237T>G GRCh38
NC_000001.10:g.68896920T>G , CM000663.1:g.68896920T>G GRCh37
NC_000001.9:g.68669508T>G NCBI36
NG_008472.1:g.23723A>C
NG_008472.2:g.23723A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1338+45A>C MANE Select ENSP00000262340.5:n.1338+45A>C
ENST00000262340.5:c.1338+45A>C ENSP00000262340.5:n.1338+45A>C
NM_000329.2:c.1338+45A>C NP_000320.1:n.1338+45A>C
XM_017002027.1:c.1062+45A>C XP_016857516.1:n.1062+45A>C
NM_000329.3:c.1338+45A>C MANE Select NP_000320.1:n.1338+45A>C