Canonical Allele Identifier: CA1624187221
Gene: PRPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722363C= , CM000668.2:g.42722363C= GRCh38
NC_000006.11:g.42690101C= , CM000668.1:g.42690101C= GRCh37
NC_000006.10:g.42798079C= NCBI36
NG_009176.1:g.5258G=
NG_009176.2:g.5258G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.-29G= MANE Select ENSP00000230381.5:n.-29G=
ENST00000230381.6:c.-29G= ENSP00000230381.5:n.-29G=
NM_000322.4:c.-29G= NP_000313.2:n.-29G=
XR_427834.2:n.627G=
XR_926295.1:n.627G=
XR_427834.4:n.677G=
XR_926295.3:n.677G=
NM_000322.5:c.-29G= MANE Select NP_000313.2:n.-29G=
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