Canonical Allele Identifier: CA902203
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs754849641
gnomAD v2: 1-68896917-G-C
gnomAD v4: 1-68431234-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431234G>C , CM000663.2:g.68431234G>C GRCh38
NC_000001.10:g.68896917G>C , CM000663.1:g.68896917G>C GRCh37
NC_000001.9:g.68669505G>C NCBI36
NG_008472.1:g.23726C>G
NG_008472.2:g.23726C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1338+48C>G MANE Select ENSP00000262340.5:n.1338+48C>G
ENST00000262340.5:c.1338+48C>G ENSP00000262340.5:n.1338+48C>G
NM_000329.2:c.1338+48C>G NP_000320.1:n.1338+48C>G
XM_017002027.1:c.1062+48C>G XP_016857516.1:n.1062+48C>G
NM_000329.3:c.1338+48C>G MANE Select NP_000320.1:n.1338+48C>G