Canonical Allele Identifier: CA738208280
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs763820730
gnomAD v3: 1-68429745-G-A
gnomAD v4: 1-68429745-G-A
MyVariant Identifiers: chr1:g.68895428G>A (hg19) chr1:g.68429745G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429745G>A , CM000663.2:g.68429745G>A GRCh38
NC_000001.10:g.68895428G>A , CM000663.1:g.68895428G>A GRCh37
NC_000001.9:g.68668016G>A NCBI36
NG_008472.1:g.25215C>T
NG_008472.2:g.25215C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*31C>T MANE Select ENSP00000262340.5:n.*31C>T
ENST00000262340.5:c.*31C>T ENSP00000262340.5:n.*31C>T
NM_000329.2:c.*31C>T NP_000320.1:n.*31C>T
XM_017002027.1:c.*31C>T XP_016857516.1:n.*31C>T
NM_000329.3:c.*31C>T MANE Select NP_000320.1:n.*31C>T
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