Canonical Allele Identifier: CA340744439
Gene: RPE65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438303A>G , CM000663.2:g.68438303A>G GRCh38
NC_000001.10:g.68903986A>G , CM000663.1:g.68903986A>G GRCh37
NC_000001.9:g.68676574A>G NCBI36
NG_008472.1:g.16657T>C
NG_008472.2:g.16657T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1012T>C MANE Select ENSP00000262340.5:p.Tyr338His
ENST00000262340.5:c.1012T>C ENSP00000262340.5:p.Tyr338His
NM_000329.2:c.1012T>C NP_000320.1:p.Tyr338His
XM_017002027.1:c.736T>C XP_016857516.1:p.Tyr246His
NM_000329.3:c.1012T>C MANE Select NP_000320.1:p.Tyr338His