Canonical Allele Identifier: CA1624187199
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722319C= , CM000668.2:g.42722319C= GRCh38
NC_000006.11:g.42690057C= , CM000668.1:g.42690057C= GRCh37
NC_000006.10:g.42798035C= NCBI36
NG_009176.1:g.5302G=
NG_009176.2:g.5302G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.16G= MANE Select ENSP00000230381.5:p.Val6=
ENST00000230381.6:c.16G= ENSP00000230381.5:p.Val6=
NM_000322.4:c.16G= NP_000313.2:p.Val6=
XR_427834.2:n.671G=
XR_926295.1:n.671G=
XR_427834.4:n.721G=
XR_926295.3:n.721G=
NM_000322.5:c.16G= MANE Select NP_000313.2:p.Val6=