Canonical Allele Identifier: CA523298727
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1441467910
gnomAD v2: 1-68895442-A-G
gnomAD v3: 1-68429759-A-G
gnomAD v4: 1-68429759-A-G
MyVariant Identifiers: chr1:g.68895442A>G (hg19) chr1:g.68429759A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429759A>G , CM000663.2:g.68429759A>G GRCh38
NC_000001.10:g.68895442A>G , CM000663.1:g.68895442A>G GRCh37
NC_000001.9:g.68668030A>G NCBI36
NG_008472.1:g.25201T>C
NG_008472.2:g.25201T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.*17T>C MANE Select ENSP00000262340.5:n.*17T>C
ENST00000262340.5:c.*17T>C ENSP00000262340.5:n.*17T>C
NM_000329.2:c.*17T>C NP_000320.1:n.*17T>C
XM_017002027.1:c.*17T>C XP_016857516.1:n.*17T>C
NM_000329.3:c.*17T>C MANE Select NP_000320.1:n.*17T>C
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