Canonical Allele Identifier: CA406381016
Community Standard Title: NC_000019.10:g.45529087G>C
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45529087G>C , CM000681.2:g.45529087G>C GRCh38
NC_000019.9:g.46032345G>C , CM000681.1:g.46032345G>C GRCh37
NC_000019.8:g.50724185G>C NCBI36
NG_013332.1:g.60778C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001017989.2:c.512C>G NP_001017989.2:p.Ala171Gly
NM_001017989.3:c.512C>G NP_001017989.2:p.Ala171Gly
ENST00000323060.3:c.512C>G ENSP00000319817.3:p.Ala171Gly
ENST00000323060.4:c.512C>G ENSP00000319817.3:p.Ala171Gly
XM_011527348.1:c.353C>G XP_011525650.1:p.Ala118Gly