Canonical Allele Identifier: CA418277575
Gene: RPE65 HGNC NCBI

Linked Data

gnomAD v4: 1-68431171-A-G
MyVariant Identifiers: chr1:g.68896854A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431171A>G , CM000663.2:g.68431171A>G GRCh38
NC_000001.10:g.68896854A>G , CM000663.1:g.68896854A>G GRCh37
NC_000001.9:g.68669442A>G NCBI36
NG_008472.1:g.23789T>C
NG_008472.2:g.23789T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1344T>C MANE Select ENSP00000262340.5:p.Cys448=
ENST00000262340.5:c.1344T>C ENSP00000262340.5:p.Cys448=
NM_000329.2:c.1344T>C NP_000320.1:p.Cys448=
XM_017002027.1:c.1068T>C XP_016857516.1:p.Cys356=
NM_000329.3:c.1344T>C MANE Select NP_000320.1:p.Cys448=