Canonical Allele Identifier: CA902198
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs764089164
gnomAD v2: 1-68896903-G-A
gnomAD v4: 1-68431220-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431220G>A , CM000663.2:g.68431220G>A GRCh38
NC_000001.10:g.68896903G>A , CM000663.1:g.68896903G>A GRCh37
NC_000001.9:g.68669491G>A NCBI36
NG_008472.1:g.23740C>T
NG_008472.2:g.23740C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1339-44C>T MANE Select ENSP00000262340.5:n.1339-44C>T
ENST00000262340.5:c.1339-44C>T ENSP00000262340.5:n.1339-44C>T
NM_000329.2:c.1339-44C>T NP_000320.1:n.1339-44C>T
XM_017002027.1:c.1063-44C>T XP_016857516.1:n.1063-44C>T
NM_000329.3:c.1339-44C>T MANE Select NP_000320.1:n.1339-44C>T