Canonical Allele Identifier: CA1624170166
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42704444C= , CM000668.2:g.42704444C= GRCh38
NC_000006.11:g.42672182C= , CM000668.1:g.42672182C= GRCh37
NC_000006.10:g.42780160C= NCBI36
NG_009176.1:g.23177G=
NG_009176.2:g.23177G=

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.749G= MANE Select ENSP00000230381.5:p.Cys250=
ENST00000230381.6:c.749G= ENSP00000230381.5:p.Cys250=
NM_000322.4:c.749G= NP_000313.2:p.Cys250=
XR_427834.2:n.1404G=
XR_427834.4:n.1454G=
XR_926295.3:n.1636G=
NM_000322.5:c.749G= MANE Select NP_000313.2:p.Cys250=