Canonical Allele Identifier: CA418277494
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68896827A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431144A>C , CM000663.2:g.68431144A>C GRCh38
NC_000001.10:g.68896827A>C , CM000663.1:g.68896827A>C GRCh37
NC_000001.9:g.68669415A>C NCBI36
NG_008472.1:g.23816T>G
NG_008472.2:g.23816T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1371T>G MANE Select ENSP00000262340.5:p.Thr457=
ENST00000262340.5:c.1371T>G ENSP00000262340.5:p.Thr457=
NM_000329.2:c.1371T>G NP_000320.1:p.Thr457=
XM_017002027.1:c.1095T>G XP_016857516.1:p.Thr365=
NM_000329.3:c.1371T>G MANE Select NP_000320.1:p.Thr457=