Canonical Allele Identifier: CA1624187170
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722266C= , CM000668.2:g.42722266C= GRCh38
NC_000006.11:g.42690004C= , CM000668.1:g.42690004C= GRCh37
NC_000006.10:g.42797982C= NCBI36
NG_009176.1:g.5355G=
NG_009176.2:g.5355G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.69G= MANE Select ENSP00000230381.5:p.Met23=
ENST00000230381.6:c.69G= ENSP00000230381.5:p.Met23=
NM_000322.4:c.69G= NP_000313.2:p.Met23=
XR_427834.2:n.724G=
XR_926295.1:n.724G=
XR_427834.4:n.774G=
XR_926295.3:n.774G=
NM_000322.5:c.69G= MANE Select NP_000313.2:p.Met23=