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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:
CA364137388
Gene: PRPH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
987409
ClinVar RCV Id:
RCV001268764
dbSNP Id:
rs61755793
MyVariant Identifiers:
chr6:g.42689558C>G (hg19)
chr6:g.42721820C>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.42721820C>G , CM000668.2:g.42721820C>G
GRCh38
NC_000006.11:g.42689558C>G , CM000668.1:g.42689558C>G
GRCh37
NC_000006.10:g.42797536C>G
NCBI36
NG_009176.1:g.5801G>C
NG_009176.2:g.5801G>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000230381.7:c.515G>C
MANE Select
ENSP00000230381.5:p.Arg172Pro
ENST00000230381.6:c.515G>C
ENSP00000230381.5:p.Arg172Pro
NM_000322.4:c.515G>C
NP_000313.2:p.Arg172Pro
XR_427834.2:n.1170G>C
XR_926295.1:n.1170G>C
XR_427834.4:n.1220G>C
XR_926295.3:n.1220G>C
NM_000322.5:c.515G>C
MANE Select
NP_000313.2:p.Arg172Pro
Search 100 bp 5'
Search 100 bp 3'