Canonical Allele Identifier: CA457569842
Gene: OPN1SW HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.128415195T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128775141T>C , CM000669.2:g.128775141T>C GRCh38
NC_000007.13:g.128415195T>C , CM000669.1:g.128415195T>C GRCh37
NC_000007.12:g.128202431T>C NCBI36
NG_009094.1:g.5650A>G
NG_033110.1:g.40850T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000249389.3:c.357A>G MANE Select ENSP00000249389.3:p.Gly119=
ENST00000249389.2:c.366A>G ENSP00000249389.2:p.Gly122=
NM_001708.2:c.366A>G NP_001699.1:p.Gly122=
NM_001385125.1:c.357A>G MANE Select NP_001372054.1:p.Gly119=
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