Canonical Allele Identifier: CA2646149569
Gene: RPE65 HGNC NCBI

Linked Data

gnomAD v4: 1-68429653-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429653T>C , CM000663.2:g.68429653T>C GRCh38
NC_000001.10:g.68895336T>C , CM000663.1:g.68895336T>C GRCh37
NC_000001.9:g.68667924T>C NCBI36
NG_008472.1:g.25307A>G
NG_008472.2:g.25307A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*123A>G MANE Select ENSP00000262340.5:n.*123A>G
ENST00000262340.5:c.*123A>G ENSP00000262340.5:n.*123A>G
NM_000329.2:c.*123A>G NP_000320.1:n.*123A>G
XM_017002027.1:c.*123A>G XP_016857516.1:n.*123A>G
NM_000329.3:c.*123A>G MANE Select NP_000320.1:n.*123A>G