Canonical Allele Identifier: CA415314635
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153457184G>C (hg19) chrX:g.154191693G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191693G>C , CM000685.2:g.154191693G>C GRCh38
NC_000023.10:g.153457184G>C , CM000685.1:g.153457184G>C GRCh37
NG_011606.1:g.14100G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.584G>C MANE Select ENSP00000472316.1:p.Trp195Ser
ENST00000595290.5:c.584G>C ENSP00000472316.1:p.Trp195Ser
ENST00000595330.1:n.588+1471G>C
ENST00000596998.2:c.171G>C
NM_000513.2:c.584G>C MANE Select NP_000504.1:p.Trp195Ser
Search 100 bp 5'
Search 100 bp 3'