Canonical Allele Identifier: CA418277650
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68896971T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431288T>G , CM000663.2:g.68431288T>G GRCh38
NC_000001.10:g.68896971T>G , CM000663.1:g.68896971T>G GRCh37
NC_000001.9:g.68669559T>G NCBI36
NG_008472.1:g.23672A>C
NG_008472.2:g.23672A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1332A>C MANE Select ENSP00000262340.5:p.Pro444=
ENST00000262340.5:c.1332A>C ENSP00000262340.5:p.Pro444=
NM_000329.2:c.1332A>C NP_000320.1:p.Pro444=
XM_017002027.1:c.1056A>C XP_016857516.1:p.Pro352=
NM_000329.3:c.1332A>C MANE Select NP_000320.1:p.Pro444=