Canonical Allele Identifier: CA2646149632
Gene: RPE65 HGNC NCBI

Linked Data

gnomAD v4: 1-68429699-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429699T>C , CM000663.2:g.68429699T>C GRCh38
NC_000001.10:g.68895382T>C , CM000663.1:g.68895382T>C GRCh37
NC_000001.9:g.68667970T>C NCBI36
NG_008472.1:g.25261A>G
NG_008472.2:g.25261A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*77A>G MANE Select ENSP00000262340.5:n.*77A>G
ENST00000262340.5:c.*77A>G ENSP00000262340.5:n.*77A>G
NM_000329.2:c.*77A>G NP_000320.1:n.*77A>G
XM_017002027.1:c.*77A>G XP_016857516.1:n.*77A>G
NM_000329.3:c.*77A>G MANE Select NP_000320.1:n.*77A>G