Canonical Allele Identifier: CA523749724
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1486351606
gnomAD v2: 1-68896947-G-T
gnomAD v4: 1-68431264-G-T
MyVariant Identifiers: chr1:g.68896947G>T (hg19) chr1:g.68431264G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431264G>T , CM000663.2:g.68431264G>T GRCh38
NC_000001.10:g.68896947G>T , CM000663.1:g.68896947G>T GRCh37
NC_000001.9:g.68669535G>T NCBI36
NG_008472.1:g.23696C>A
NG_008472.2:g.23696C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1338+18C>A MANE Select ENSP00000262340.5:n.1338+18C>A
ENST00000262340.5:c.1338+18C>A ENSP00000262340.5:n.1338+18C>A
NM_000329.2:c.1338+18C>A NP_000320.1:n.1338+18C>A
XM_017002027.1:c.1062+18C>A XP_016857516.1:n.1062+18C>A
NM_000329.3:c.1338+18C>A MANE Select NP_000320.1:n.1338+18C>A
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