Canonical Allele Identifier: CA1624187161
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722252A= , CM000668.2:g.42722252A= GRCh38
NC_000006.11:g.42689990A= , CM000668.1:g.42689990A= GRCh37
NC_000006.10:g.42797968A= NCBI36
NG_009176.1:g.5369T=
NG_009176.2:g.5369T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.83T= MANE Select ENSP00000230381.5:p.Val28=
ENST00000230381.6:c.83T= ENSP00000230381.5:p.Val28=
NM_000322.4:c.83T= NP_000313.2:p.Val28=
XR_427834.2:n.738T=
XR_926295.1:n.738T=
XR_427834.4:n.788T=
XR_926295.3:n.788T=
NM_000322.5:c.83T= MANE Select NP_000313.2:p.Val28=