Canonical Allele Identifier: CA340748209
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68910488G>C (hg19) chr1:g.68444805G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444805G>C , CM000663.2:g.68444805G>C GRCh38
NC_000001.10:g.68910488G>C , CM000663.1:g.68910488G>C GRCh37
NC_000001.9:g.68683076G>C NCBI36
NG_008472.1:g.10155C>G
NG_008472.2:g.10155C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.324C>G MANE Select ENSP00000262340.5:p.Phe108Leu
ENST00000262340.5:c.324C>G ENSP00000262340.5:p.Phe108Leu
NM_000329.2:c.324C>G NP_000320.1:p.Phe108Leu
XM_017002027.1:c.48C>G XP_016857516.1:p.Phe16Leu
NM_000329.3:c.324C>G MANE Select NP_000320.1:p.Phe108Leu
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