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Canonical Allele Identifier:
CA406381022
Community Standard Title: NC_000019.10:g.45529088C>T
Gene: OPA3
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.45529088C>T , CM000681.2:g.45529088C>T
GRCh38
NC_000019.9:g.46032346C>T , CM000681.1:g.46032346C>T
GRCh37
NC_000019.8:g.50724186C>T
NCBI36
NG_013332.1:g.60777G>A
Transcript Alleles
HGVS
Amino-acid Change
NM_001017989.2:c.511G>A
NP_001017989.2:p.Ala171Thr
NM_001017989.3:c.511G>A
NP_001017989.2:p.Ala171Thr
ENST00000323060.3:c.511G>A
ENSP00000319817.3:p.Ala171Thr
ENST00000323060.4:c.511G>A
ENSP00000319817.3:p.Ala171Thr
XM_011527348.1:c.352G>A
XP_011525650.1:p.Ala118Thr
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