Canonical Allele Identifier: CA1173564228
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68446746A= , CM000663.2:g.68446746A= GRCh38
NC_000001.10:g.68912429A= , CM000663.1:g.68912429A= GRCh37
NC_000001.9:g.68685017A= NCBI36
NG_008472.1:g.8214T=
NG_008472.2:g.8214T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.209T= MANE Select ENSP00000262340.5:p.Phe70=
ENST00000262340.5:c.209T= ENSP00000262340.5:p.Phe70=
NM_000329.2:c.209T= NP_000320.1:p.Phe70=
XM_017002027.1:c.-31-1863T= XP_016857516.1:n.-31-1863T=
NM_000329.3:c.209T= MANE Select NP_000320.1:p.Phe70=