Canonical Allele Identifier: CA418279798
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1645880052
gnomAD v3: 1-68438989-G-C
gnomAD v4: 1-68438989-G-C
MyVariant Identifiers: chr1:g.68904672G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438989G>C , CM000663.2:g.68438989G>C GRCh38
NC_000001.10:g.68904672G>C , CM000663.1:g.68904672G>C GRCh37
NC_000001.9:g.68677260G>C NCBI36
NG_008472.1:g.15971C>G
NG_008472.2:g.15971C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.951C>G MANE Select ENSP00000262340.5:p.Thr317=
ENST00000262340.5:c.951C>G ENSP00000262340.5:p.Thr317=
NM_000329.2:c.951C>G NP_000320.1:p.Thr317=
XM_017002027.1:c.675C>G XP_016857516.1:p.Thr225=
NM_000329.3:c.951C>G MANE Select NP_000320.1:p.Thr317=