Canonical Allele Identifier: CA902213
Gene: RPE65 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1297T>A MANE Select ENSP00000262340.5:p.Tyr433Asn
ENST00000262340.5:c.1297T>A ENSP00000262340.5:p.Tyr433Asn
NM_000329.2:c.1297T>A NP_000320.1:p.Tyr433Asn
XM_017002027.1:c.1021T>A XP_016857516.1:p.Tyr341Asn
NM_000329.3:c.1297T>A MANE Select NP_000320.1:p.Tyr433Asn