Canonical Allele Identifier: CA450362701
Gene: PRPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.42689959T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722221T>G , CM000668.2:g.42722221T>G GRCh38
NC_000006.11:g.42689959T>G , CM000668.1:g.42689959T>G GRCh37
NC_000006.10:g.42797937T>G NCBI36
NG_009176.1:g.5400A>C
NG_009176.2:g.5400A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.114A>C MANE Select ENSP00000230381.5:p.Gly38=
ENST00000230381.6:c.114A>C ENSP00000230381.5:p.Gly38=
NM_000322.4:c.114A>C NP_000313.2:p.Gly38=
XR_427834.2:n.769A>C
XR_926295.1:n.769A>C
XR_427834.4:n.819A>C
XR_926295.3:n.819A>C
NM_000322.5:c.114A>C MANE Select NP_000313.2:p.Gly38=
Search 100 bp 5'
Search 100 bp 3'