Canonical Allele Identifier: CA406381007
Community Standard Title: NC_000019.10:g.45529085G>C
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45529085G>C , CM000681.2:g.45529085G>C GRCh38
NC_000019.9:g.46032343G>C , CM000681.1:g.46032343G>C GRCh37
NC_000019.8:g.50724183G>C NCBI36
NG_013332.1:g.60780C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001017989.2:c.514C>G NP_001017989.2:p.Pro172Ala
NM_001017989.3:c.514C>G NP_001017989.2:p.Pro172Ala
ENST00000323060.3:c.514C>G ENSP00000319817.3:p.Pro172Ala
ENST00000323060.4:c.514C>G ENSP00000319817.3:p.Pro172Ala
XM_011527348.1:c.355C>G XP_011525650.1:p.Pro119Ala