Canonical Allele Identifier: CA1624170291
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42704509G= , CM000668.2:g.42704509G= GRCh38
NC_000006.11:g.42672247G= , CM000668.1:g.42672247G= GRCh37
NC_000006.10:g.42780225G= NCBI36
NG_009176.1:g.23112C=
NG_009176.2:g.23112C=

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.684C= MANE Select ENSP00000230381.5:p.Thr228=
ENST00000230381.6:c.684C= ENSP00000230381.5:p.Thr228=
NM_000322.4:c.684C= NP_000313.2:p.Thr228=
XR_427834.2:n.1339C=
XR_427834.4:n.1389C=
XR_926295.3:n.1571C=
NM_000322.5:c.684C= MANE Select NP_000313.2:p.Thr228=