Canonical Allele Identifier: CA1624187176
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722280C= , CM000668.2:g.42722280C= GRCh38
NC_000006.11:g.42690018C= , CM000668.1:g.42690018C= GRCh37
NC_000006.10:g.42797996C= NCBI36
NG_009176.1:g.5341G=
NG_009176.2:g.5341G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.55G= MANE Select ENSP00000230381.5:p.Gly19=
ENST00000230381.6:c.55G= ENSP00000230381.5:p.Gly19=
NM_000322.4:c.55G= NP_000313.2:p.Gly19=
XR_427834.2:n.710G=
XR_926295.1:n.710G=
XR_427834.4:n.760G=
XR_926295.3:n.760G=
NM_000322.5:c.55G= MANE Select NP_000313.2:p.Gly19=