Canonical Allele Identifier: CA519323128
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153420214G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154154739G>C , CM000685.2:g.154154739G>C GRCh38
NC_000023.10:g.153420214G>C , CM000685.1:g.153420214G>C GRCh37
NC_000023.9:g.153073408G>C NCBI36
NG_009105.2:g.15489G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.744G>C MANE Select ENSP00000358967.4:p.Ala248=
ENST00000369951.8:c.744G>C ENSP00000358967.4:p.Ala248=
ENST00000442922.1:c.333G>C ENSP00000402493.1:p.Ala111=
ENST00000463296.1:n.589-1555G>C
NM_020061.5:c.744G>C NP_064445.2:p.Ala248=
NM_020061.6:c.744G>C MANE Select NP_064445.2:p.Ala248=
Search 100 bp 5'
Search 100 bp 3'