Canonical Allele Identifier: CA1624187188
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722295C= , CM000668.2:g.42722295C= GRCh38
NC_000006.11:g.42690033C= , CM000668.1:g.42690033C= GRCh37
NC_000006.10:g.42798011C= NCBI36
NG_009176.1:g.5326G=
NG_009176.2:g.5326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.40G= MANE Select ENSP00000230381.5:p.Val14=
ENST00000230381.6:c.40G= ENSP00000230381.5:p.Val14=
NM_000322.4:c.40G= NP_000313.2:p.Val14=
XR_427834.2:n.695G=
XR_926295.1:n.695G=
XR_427834.4:n.745G=
XR_926295.3:n.745G=
NM_000322.5:c.40G= MANE Select NP_000313.2:p.Val14=