Canonical Allele Identifier: CA340742198
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68896831T>C (hg19) chr1:g.68431148T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431148T>C , CM000663.2:g.68431148T>C GRCh38
NC_000001.10:g.68896831T>C , CM000663.1:g.68896831T>C GRCh37
NC_000001.9:g.68669419T>C NCBI36
NG_008472.1:g.23812A>G
NG_008472.2:g.23812A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1367A>G MANE Select ENSP00000262340.5:p.Glu456Gly
ENST00000262340.5:c.1367A>G ENSP00000262340.5:p.Glu456Gly
NM_000329.2:c.1367A>G NP_000320.1:p.Glu456Gly
XM_017002027.1:c.1091A>G XP_016857516.1:p.Glu364Gly
NM_000329.3:c.1367A>G MANE Select NP_000320.1:p.Glu456Gly
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