Canonical Allele Identifier: CA23562741
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1006868300
MyVariant Identifiers: chr1:g.68430085C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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