Canonical Allele Identifier: CA1624187193
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722305C= , CM000668.2:g.42722305C= GRCh38
NC_000006.11:g.42690043C= , CM000668.1:g.42690043C= GRCh37
NC_000006.10:g.42798021C= NCBI36
NG_009176.1:g.5316G=
NG_009176.2:g.5316G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.30G= MANE Select ENSP00000230381.5:p.Gln10=
ENST00000230381.6:c.30G= ENSP00000230381.5:p.Gln10=
NM_000322.4:c.30G= NP_000313.2:p.Gln10=
XR_427834.2:n.685G=
XR_926295.1:n.685G=
XR_427834.4:n.735G=
XR_926295.3:n.735G=
NM_000322.5:c.30G= MANE Select NP_000313.2:p.Gln10=