Canonical Allele Identifier: CA902194
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs759868752
gnomAD v2: 1-68896884-T-C
gnomAD v3: 1-68431201-T-C
gnomAD v4: 1-68431201-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431201T>C , CM000663.2:g.68431201T>C GRCh38
NC_000001.10:g.68896884T>C , CM000663.1:g.68896884T>C GRCh37
NC_000001.9:g.68669472T>C NCBI36
NG_008472.1:g.23759A>G
NG_008472.2:g.23759A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1339-25A>G MANE Select ENSP00000262340.5:n.1339-25A>G
ENST00000262340.5:c.1339-25A>G ENSP00000262340.5:n.1339-25A>G
NM_000329.2:c.1339-25A>G NP_000320.1:n.1339-25A>G
XM_017002027.1:c.1063-25A>G XP_016857516.1:n.1063-25A>G
NM_000329.3:c.1339-25A>G MANE Select NP_000320.1:n.1339-25A>G