Canonical Allele Identifier: CA1624187181
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722286C= , CM000668.2:g.42722286C= GRCh38
NC_000006.11:g.42690024C= , CM000668.1:g.42690024C= GRCh37
NC_000006.10:g.42798002C= NCBI36
NG_009176.1:g.5335G=
NG_009176.2:g.5335G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.49G= MANE Select ENSP00000230381.5:p.Ala17=
ENST00000230381.6:c.49G= ENSP00000230381.5:p.Ala17=
NM_000322.4:c.49G= NP_000313.2:p.Ala17=
XR_427834.2:n.704G=
XR_926295.1:n.704G=
XR_427834.4:n.754G=
XR_926295.3:n.754G=
NM_000322.5:c.49G= MANE Select NP_000313.2:p.Ala17=