Canonical Allele Identifier: CA146043
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 92859
dbSNP Id: rs61752901
gnomAD v2: 1-68904742-T-G
gnomAD v3: 1-68439059-T-G
gnomAD v4: 1-68439059-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68439059T>G , CM000663.2:g.68439059T>G GRCh38
NC_000001.10:g.68904742T>G , CM000663.1:g.68904742T>G GRCh37
NC_000001.9:g.68677330T>G NCBI36
NG_008472.1:g.15901A>C
NG_008472.2:g.15901A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.881A>C MANE Select ENSP00000262340.5:p.Lys294Thr
ENST00000262340.5:c.881A>C ENSP00000262340.5:p.Lys294Thr
NM_000329.2:c.881A>C NP_000320.1:p.Lys294Thr
XM_017002027.1:c.605A>C XP_016857516.1:p.Lys202Thr
NM_000329.3:c.881A>C MANE Select NP_000320.1:p.Lys294Thr