Canonical Allele Identifier: CA418276138
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68895516C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429833C>A , CM000663.2:g.68429833C>A GRCh38
NC_000001.10:g.68895516C>A , CM000663.1:g.68895516C>A GRCh37
NC_000001.9:g.68668104C>A NCBI36
NG_008472.1:g.25127G>T
NG_008472.2:g.25127G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.1545G>T MANE Select ENSP00000262340.5:p.Arg515=
ENST00000262340.5:c.1545G>T ENSP00000262340.5:p.Arg515=
NM_000329.2:c.1545G>T NP_000320.1:p.Arg515=
XM_017002027.1:c.1269G>T XP_016857516.1:p.Arg423=
NM_000329.3:c.1545G>T MANE Select NP_000320.1:p.Arg515=
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