Canonical Allele Identifier: CA523298934
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1006868300
gnomAD v2: 1-68895768-C-A
gnomAD v3: 1-68430085-C-A
gnomAD v4: 1-68430085-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430085C>A , CM000663.2:g.68430085C>A GRCh38
NC_000001.10:g.68895768C>A , CM000663.1:g.68895768C>A GRCh37
NC_000001.9:g.68668356C>A NCBI36
NG_008472.1:g.24875G>T
NG_008472.2:g.24875G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-158G>T MANE Select ENSP00000262340.5:n.1451-158G>T
ENST00000262340.5:c.1451-158G>T ENSP00000262340.5:n.1451-158G>T
NM_000329.2:c.1451-158G>T NP_000320.1:n.1451-158G>T
XM_017002027.1:c.1175-158G>T XP_016857516.1:n.1175-158G>T
NM_000329.3:c.1451-158G>T MANE Select NP_000320.1:n.1451-158G>T