Canonical Allele Identifier: CA2695997467
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs2100805612

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430121T>C , CM000663.2:g.68430121T>C GRCh38
NC_000001.10:g.68895804T>C , CM000663.1:g.68895804T>C GRCh37
NC_000001.9:g.68668392T>C NCBI36
NG_008472.1:g.24839A>G
NG_008472.2:g.24839A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-194A>G MANE Select ENSP00000262340.5:n.1451-194A>G
ENST00000262340.5:c.1451-194A>G ENSP00000262340.5:n.1451-194A>G
NM_000329.2:c.1451-194A>G NP_000320.1:n.1451-194A>G
XM_017002027.1:c.1175-194A>G XP_016857516.1:n.1175-194A>G
NM_000329.3:c.1451-194A>G MANE Select NP_000320.1:n.1451-194A>G