Canonical Allele Identifier: CA418277702
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68896989G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431306G>C , CM000663.2:g.68431306G>C GRCh38
NC_000001.10:g.68896989G>C , CM000663.1:g.68896989G>C GRCh37
NC_000001.9:g.68669577G>C NCBI36
NG_008472.1:g.23654C>G
NG_008472.2:g.23654C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1314C>G MANE Select ENSP00000262340.5:p.Gly438=
ENST00000262340.5:c.1314C>G ENSP00000262340.5:p.Gly438=
NM_000329.2:c.1314C>G NP_000320.1:p.Gly438=
XM_017002027.1:c.1038C>G XP_016857516.1:p.Gly346=
NM_000329.3:c.1314C>G MANE Select NP_000320.1:p.Gly438=