Canonical Allele Identifier: CA738209723
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1381993829

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431447G>C , CM000663.2:g.68431447G>C GRCh38
NC_000001.10:g.68897130G>C , CM000663.1:g.68897130G>C GRCh37
NC_000001.9:g.68669718G>C NCBI36
NG_008472.1:g.23513C>G
NG_008472.2:g.23513C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+24C>G MANE Select ENSP00000262340.5:n.1243+24C>G
ENST00000262340.5:c.1243+24C>G ENSP00000262340.5:n.1243+24C>G
NM_000329.2:c.1243+24C>G NP_000320.1:n.1243+24C>G
XM_017002027.1:c.967+24C>G XP_016857516.1:n.967+24C>G
NM_000329.3:c.1243+24C>G MANE Select NP_000320.1:n.1243+24C>G