Canonical Allele Identifier: CA418277504
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68896830T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431147T>C , CM000663.2:g.68431147T>C GRCh38
NC_000001.10:g.68896830T>C , CM000663.1:g.68896830T>C GRCh37
NC_000001.9:g.68669418T>C NCBI36
NG_008472.1:g.23813A>G
NG_008472.2:g.23813A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1368A>G MANE Select ENSP00000262340.5:p.Glu456=
ENST00000262340.5:c.1368A>G ENSP00000262340.5:p.Glu456=
NM_000329.2:c.1368A>G NP_000320.1:p.Glu456=
XM_017002027.1:c.1092A>G XP_016857516.1:p.Glu364=
NM_000329.3:c.1368A>G MANE Select NP_000320.1:p.Glu456=