Canonical Allele Identifier: CA2646150280
Gene: RPE65 HGNC NCBI

Linked Data

gnomAD v4: 1-68431420-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431420G>T , CM000663.2:g.68431420G>T GRCh38
NC_000001.10:g.68897103G>T , CM000663.1:g.68897103G>T GRCh37
NC_000001.9:g.68669691G>T NCBI36
NG_008472.1:g.23540C>A
NG_008472.2:g.23540C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1244-44C>A MANE Select ENSP00000262340.5:n.1244-44C>A
ENST00000262340.5:c.1244-44C>A ENSP00000262340.5:n.1244-44C>A
NM_000329.2:c.1244-44C>A NP_000320.1:n.1244-44C>A
XM_017002027.1:c.968-44C>A XP_016857516.1:n.968-44C>A
NM_000329.3:c.1244-44C>A MANE Select NP_000320.1:n.1244-44C>A