Canonical Allele Identifier: CA1624187198
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722317G= , CM000668.2:g.42722317G= GRCh38
NC_000006.11:g.42690055G= , CM000668.1:g.42690055G= GRCh37
NC_000006.10:g.42798033G= NCBI36
NG_009176.1:g.5304C=
NG_009176.2:g.5304C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.18C= MANE Select ENSP00000230381.5:p.Val6=
ENST00000230381.6:c.18C= ENSP00000230381.5:p.Val6=
NM_000322.4:c.18C= NP_000313.2:p.Val6=
XR_427834.2:n.673C=
XR_926295.1:n.673C=
XR_427834.4:n.723C=
XR_926295.3:n.723C=
NM_000322.5:c.18C= MANE Select NP_000313.2:p.Val6=