Canonical Allele Identifier: CA415313748
Gene: OPN1MW HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154188022G>T , CM000685.2:g.154188022G>T GRCh38
NC_000023.10:g.153453511G>T , CM000685.1:g.153453511G>T GRCh37
NG_011606.1:g.10427G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.365G>T MANE Select ENSP00000472316.1:p.Gly122Val
ENST00000595290.5:c.365G>T ENSP00000472316.1:p.Gly122Val
ENST00000595330.1:n.375G>T
NM_000513.2:c.365G>T MANE Select NP_000504.1:p.Gly122Val