Canonical Allele Identifier: CA418278219
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs2100807734
MyVariant Identifiers: chr1:g.68897155T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431472T>C , CM000663.2:g.68431472T>C GRCh38
NC_000001.10:g.68897155T>C , CM000663.1:g.68897155T>C GRCh37
NC_000001.9:g.68669743T>C NCBI36
NG_008472.1:g.23488A>G
NG_008472.2:g.23488A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1242A>G MANE Select ENSP00000262340.5:p.Gln414=
ENST00000262340.5:c.1242A>G ENSP00000262340.5:p.Gln414=
NM_000329.2:c.1242A>G NP_000320.1:p.Gln414=
XM_017002027.1:c.966A>G XP_016857516.1:p.Gln322=
NM_000329.3:c.1242A>G MANE Select NP_000320.1:p.Gln414=