Canonical Allele Identifier: CA1002830231
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1489591456
gnomAD v3: 1-68429672-A-G
gnomAD v4: 1-68429672-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429672A>G , CM000663.2:g.68429672A>G GRCh38
NC_000001.10:g.68895355A>G , CM000663.1:g.68895355A>G GRCh37
NC_000001.9:g.68667943A>G NCBI36
NG_008472.1:g.25288T>C
NG_008472.2:g.25288T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*104T>C MANE Select ENSP00000262340.5:n.*104T>C
ENST00000262340.5:c.*104T>C ENSP00000262340.5:n.*104T>C
NM_000329.2:c.*104T>C NP_000320.1:n.*104T>C
XM_017002027.1:c.*104T>C XP_016857516.1:n.*104T>C
NM_000329.3:c.*104T>C MANE Select NP_000320.1:n.*104T>C