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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA369220944
Gene: OPN1SW
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr7:g.128415200T>A (hg19)
chr7:g.128775146T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.128775146T>A , CM000669.2:g.128775146T>A
GRCh38
NC_000007.13:g.128415200T>A , CM000669.1:g.128415200T>A
GRCh37
NC_000007.12:g.128202436T>A
NCBI36
NG_009094.1:g.5645A>T
NG_033110.1:g.40855T>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000249389.3:c.352A>T
MANE Select
ENSP00000249389.3:p.Thr118Ser
ENST00000249389.2:c.361A>T
ENSP00000249389.2:p.Thr121Ser
NM_001708.2:c.361A>T
NP_001699.1:p.Thr121Ser
NM_001385125.1:c.352A>T
MANE Select
NP_001372054.1:p.Thr118Ser
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