Canonical Allele Identifier: CA418276122
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68895510T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429827T>C , CM000663.2:g.68429827T>C GRCh38
NC_000001.10:g.68895510T>C , CM000663.1:g.68895510T>C GRCh37
NC_000001.9:g.68668098T>C NCBI36
NG_008472.1:g.25133A>G
NG_008472.2:g.25133A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.1551A>G MANE Select ENSP00000262340.5:p.Glu517=
ENST00000262340.5:c.1551A>G ENSP00000262340.5:p.Glu517=
NM_000329.2:c.1551A>G NP_000320.1:p.Glu517=
XM_017002027.1:c.1275A>G XP_016857516.1:p.Glu425=
NM_000329.3:c.1551A>G MANE Select NP_000320.1:p.Glu517=
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