Canonical Allele Identifier: CA340742928
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1235881190
gnomAD v2: 1-68897168-G-C
gnomAD v4: 1-68431485-G-C
MyVariant Identifiers: chr1:g.68897168G>C (hg19) chr1:g.68431485G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431485G>C , CM000663.2:g.68431485G>C GRCh38
NC_000001.10:g.68897168G>C , CM000663.1:g.68897168G>C GRCh37
NC_000001.9:g.68669756G>C NCBI36
NG_008472.1:g.23475C>G
NG_008472.2:g.23475C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1229C>G MANE Select ENSP00000262340.5:p.Ser410Ter
ENST00000262340.5:c.1229C>G ENSP00000262340.5:p.Ser410Ter
NM_000329.2:c.1229C>G NP_000320.1:p.Ser410Ter
XM_017002027.1:c.953C>G XP_016857516.1:p.Ser318Ter
NM_000329.3:c.1229C>G MANE Select NP_000320.1:p.Ser410Ter
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