Canonical Allele Identifier: CA1624186861
Gene: PRPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721604C= , CM000668.2:g.42721604C= GRCh38
NC_000006.11:g.42689342C= , CM000668.1:g.42689342C= GRCh37
NC_000006.10:g.42797320C= NCBI36
NG_009176.1:g.6017G=
NG_009176.2:g.6017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.581+150G= MANE Select ENSP00000230381.5:n.581+150G=
ENST00000230381.6:c.581+150G= ENSP00000230381.5:n.581+150G=
NM_000322.4:c.581+150G= NP_000313.2:n.581+150G=
XR_427834.2:n.1236+150G=
XR_926295.1:n.1236+150G=
XR_427834.4:n.1286+150G=
XR_926295.3:n.1286+150G=
NM_000322.5:c.581+150G= MANE Select NP_000313.2:n.581+150G=
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