Canonical Allele Identifier: CA340747654
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68910260T>G (hg19) chr1:g.68444577T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444577T>G , CM000663.2:g.68444577T>G GRCh38
NC_000001.10:g.68910260T>G , CM000663.1:g.68910260T>G GRCh37
NC_000001.9:g.68682848T>G NCBI36
NG_008472.1:g.10383A>C
NG_008472.2:g.10383A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.449A>C MANE Select ENSP00000262340.5:p.Asn150Thr
ENST00000262340.5:c.449A>C ENSP00000262340.5:p.Asn150Thr
NM_000329.2:c.449A>C NP_000320.1:p.Asn150Thr
XM_017002027.1:c.173A>C XP_016857516.1:p.Asn58Thr
NM_000329.3:c.449A>C MANE Select NP_000320.1:p.Asn150Thr
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