Canonical Allele Identifier: CA1624170724
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42704618G= , CM000668.2:g.42704618G= GRCh38
NC_000006.11:g.42672356G= , CM000668.1:g.42672356G= GRCh37
NC_000006.10:g.42780334G= NCBI36
NG_009176.1:g.23003C=
NG_009176.2:g.23003C=

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.582-7C= MANE Select ENSP00000230381.5:n.582-7C=
ENST00000230381.6:c.582-7C= ENSP00000230381.5:n.582-7C=
NM_000322.4:c.582-7C= NP_000313.2:n.582-7C=
XR_427834.2:n.1237-7C=
XR_926295.1:n.1419-7C=
XR_427834.4:n.1287-7C=
XR_926295.3:n.1469-7C=
NM_000322.5:c.582-7C= MANE Select NP_000313.2:n.582-7C=