Canonical Allele Identifier: CA418282699
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68910265C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444582C>T , CM000663.2:g.68444582C>T GRCh38
NC_000001.10:g.68910265C>T , CM000663.1:g.68910265C>T GRCh37
NC_000001.9:g.68682853C>T NCBI36
NG_008472.1:g.10378G>A
NG_008472.2:g.10378G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.444G>A MANE Select ENSP00000262340.5:p.Glu148=
ENST00000262340.5:c.444G>A ENSP00000262340.5:p.Glu148=
NM_000329.2:c.444G>A NP_000320.1:p.Glu148=
XM_017002027.1:c.168G>A XP_016857516.1:p.Glu56=
NM_000329.3:c.444G>A MANE Select NP_000320.1:p.Glu148=
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