Canonical Allele Identifier: CA2580063207
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962564

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431179G>C , CM000663.2:g.68431179G>C GRCh38
NC_000001.10:g.68896862G>C , CM000663.1:g.68896862G>C GRCh37
NC_000001.9:g.68669450G>C NCBI36
NG_008472.1:g.23781C>G
NG_008472.2:g.23781C>G

Transcript Alleles

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