Canonical Allele Identifier: CA1173561341
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1645885069
gnomAD v4: 1-68439499-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68439499T>A , CM000663.2:g.68439499T>A GRCh38
NC_000001.10:g.68905182T>A , CM000663.1:g.68905182T>A GRCh37
NC_000001.9:g.68677770T>A NCBI36
NG_008472.1:g.15461A>T
NG_008472.2:g.15461A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.725+62A>T MANE Select ENSP00000262340.5:n.725+62A>T
ENST00000262340.5:c.725+62A>T ENSP00000262340.5:n.725+62A>T
NM_000329.2:c.725+62A>T NP_000320.1:n.725+62A>T
XM_017002027.1:c.449+62A>T XP_016857516.1:n.449+62A>T
NM_000329.3:c.725+62A>T MANE Select NP_000320.1:n.725+62A>T
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