Canonical Allele Identifier: CA340748034
Gene: RPE65 HGNC NCBI

Linked Data

gnomAD v4: 1-68444672-C-G
MyVariant Identifiers: chr1:g.68910355C>G (hg19) chr1:g.68444672C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444672C>G , CM000663.2:g.68444672C>G GRCh38
NC_000001.10:g.68910355C>G , CM000663.1:g.68910355C>G GRCh37
NC_000001.9:g.68682943C>G NCBI36
NG_008472.1:g.10288G>C
NG_008472.2:g.10288G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.354G>C MANE Select ENSP00000262340.5:p.Arg118Ser
ENST00000262340.5:c.354G>C ENSP00000262340.5:p.Arg118Ser
NM_000329.2:c.354G>C NP_000320.1:p.Arg118Ser
XM_017002027.1:c.78G>C XP_016857516.1:p.Arg26Ser
NM_000329.3:c.354G>C MANE Select NP_000320.1:p.Arg118Ser
Search 100 bp 5'
Search 100 bp 3'