Canonical Allele Identifier: CA1624187190
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722298G= , CM000668.2:g.42722298G= GRCh38
NC_000006.11:g.42690036G= , CM000668.1:g.42690036G= GRCh37
NC_000006.10:g.42798014G= NCBI36
NG_009176.1:g.5323C=
NG_009176.2:g.5323C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.37C= MANE Select ENSP00000230381.5:p.Arg13=
ENST00000230381.6:c.37C= ENSP00000230381.5:p.Arg13=
NM_000322.4:c.37C= NP_000313.2:p.Arg13=
XR_427834.2:n.692C=
XR_926295.1:n.692C=
XR_427834.4:n.742C=
XR_926295.3:n.742C=
NM_000322.5:c.37C= MANE Select NP_000313.2:p.Arg13=