Canonical Allele Identifier: CA226597
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 98903
dbSNP Id: rs61752907
gnomAD v2: 1-68904645-C-A
gnomAD v3: 1-68438962-C-A
gnomAD v4: 1-68438962-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438962C>A , CM000663.2:g.68438962C>A GRCh38
NC_000001.10:g.68904645C>A , CM000663.1:g.68904645C>A GRCh37
NC_000001.9:g.68677233C>A NCBI36
NG_008472.1:g.15998G>T
NG_008472.2:g.15998G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.978G>T MANE Select ENSP00000262340.5:p.Val326=
ENST00000262340.5:c.978G>T ENSP00000262340.5:p.Val326=
NM_000329.2:c.978G>T NP_000320.1:p.Val326=
XM_017002027.1:c.702G>T XP_016857516.1:p.Val234=
NM_000329.3:c.978G>T MANE Select NP_000320.1:p.Val326=