Canonical Allele Identifier: CA10558846
Gene: OPN1LW HGNC NCBI

Linked Data

dbSNP Id: rs782452318
ExAC: X:153419998 C / T
gnomAD v2: X-153419998-C-T
gnomAD v4: X-154154523-C-T
MyVariant Identifiers: chrX:g.153419998C>T (hg19) chrX:g.154154523C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154154523C>T , CM000685.2:g.154154523C>T GRCh38
NC_000023.10:g.153419998C>T , CM000685.1:g.153419998C>T GRCh37
NC_000023.9:g.153073192C>T NCBI36
NG_009105.2:g.15273C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.579-51C>T MANE Select ENSP00000358967.4:n.579-51C>T
ENST00000369951.8:c.579-51C>T ENSP00000358967.4:n.579-51C>T
ENST00000442922.1:c.168-51C>T ENSP00000402493.1:n.168-51C>T
ENST00000463296.1:n.588+1415C>T
NM_020061.5:c.579-51C>T NP_064445.2:n.579-51C>T
NM_020061.6:c.579-51C>T MANE Select NP_064445.2:n.579-51C>T
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