Canonical Allele Identifier: CA523298725
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1377520914
gnomAD v2: 1-68895382-T-A
MyVariant Identifiers: chr1:g.68895382T>A (hg19) chr1:g.68429699T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429699T>A , CM000663.2:g.68429699T>A GRCh38
NC_000001.10:g.68895382T>A , CM000663.1:g.68895382T>A GRCh37
NC_000001.9:g.68667970T>A NCBI36
NG_008472.1:g.25261A>T
NG_008472.2:g.25261A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*77A>T MANE Select ENSP00000262340.5:n.*77A>T
ENST00000262340.5:c.*77A>T ENSP00000262340.5:n.*77A>T
NM_000329.2:c.*77A>T NP_000320.1:n.*77A>T
XM_017002027.1:c.*77A>T XP_016857516.1:n.*77A>T
NM_000329.3:c.*77A>T MANE Select NP_000320.1:n.*77A>T
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