Canonical Allele Identifier: CA902214
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs774624260
gnomAD v2: 1-68897006-A-G
gnomAD v4: 1-68431323-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431323A>G , CM000663.2:g.68431323A>G GRCh38
NC_000001.10:g.68897006A>G , CM000663.1:g.68897006A>G GRCh37
NC_000001.9:g.68669594A>G NCBI36
NG_008472.1:g.23637T>C
NG_008472.2:g.23637T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1297T>C MANE Select ENSP00000262340.5:p.Tyr433His
ENST00000262340.5:c.1297T>C ENSP00000262340.5:p.Tyr433His
NM_000329.2:c.1297T>C NP_000320.1:p.Tyr433His
XM_017002027.1:c.1021T>C XP_016857516.1:p.Tyr341His
NM_000329.3:c.1297T>C MANE Select NP_000320.1:p.Tyr433His