Canonical Allele Identifier: CA340747636

Gene: RPE65

Linked Data

• dbSNP Id: rs1645927697
• MyVariant Identifiers: chr1:g.68910258A>G (hg19) ; chr1:g.68444575A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.68444575A>G , CM000663.2:g.68444575A>G	GRCh38
NC_000001.10:g.68910258A>G , CM000663.1:g.68910258A>G	GRCh37
NC_000001.9:g.68682846A>G	NCBI36
NG_008472.1:g.10385T>C
NG_008472.2:g.10385T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262340.6:c.451T>C MANE Select	ENSP00000262340.5:p.Phe151Leu
ENST00000262340.5:c.451T>C	ENSP00000262340.5:p.Phe151Leu
NM_000329.2:c.451T>C	NP_000320.1:p.Phe151Leu
XM_017002027.1:c.175T>C	XP_016857516.1:p.Phe59Leu
NM_000329.3:c.451T>C MANE Select	NP_000320.1:p.Phe151Leu