Canonical Allele Identifier: CA138186975
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 971644
ClinVar RCV Id: RCV001247474
dbSNP Id: rs960152679
gnomAD v4: 6-42721787-C-T
MyVariant Identifiers: chr6:g.42689525C>T (hg19) chr6:g.42721787C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721787C>T , CM000668.2:g.42721787C>T GRCh38
NC_000006.11:g.42689525C>T , CM000668.1:g.42689525C>T GRCh37
NC_000006.10:g.42797503C>T NCBI36
NG_009176.1:g.5834G>A
NG_009176.2:g.5834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.548G>A MANE Select ENSP00000230381.5:p.Arg183His
ENST00000230381.6:c.548G>A ENSP00000230381.5:p.Arg183His
NM_000322.4:c.548G>A NP_000313.2:p.Arg183His
XR_427834.2:n.1203G>A
XR_926295.1:n.1203G>A
XR_427834.4:n.1253G>A
XR_926295.3:n.1253G>A
NM_000322.5:c.548G>A MANE Select NP_000313.2:p.Arg183His
Search 100 bp 5'
Search 100 bp 3'