Canonical Allele Identifier: CA1624187158
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722240A= , CM000668.2:g.42722240A= GRCh38
NC_000006.11:g.42689978A= , CM000668.1:g.42689978A= GRCh37
NC_000006.10:g.42797956A= NCBI36
NG_009176.1:g.5381T=
NG_009176.2:g.5381T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.95T= MANE Select ENSP00000230381.5:p.Ile32=
ENST00000230381.6:c.95T= ENSP00000230381.5:p.Ile32=
NM_000322.4:c.95T= NP_000313.2:p.Ile32=
XR_427834.2:n.750T=
XR_926295.1:n.750T=
XR_427834.4:n.800T=
XR_926295.3:n.800T=
NM_000322.5:c.95T= MANE Select NP_000313.2:p.Ile32=