Canonical Allele Identifier: CA1624187210
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722345T= , CM000668.2:g.42722345T= GRCh38
NC_000006.11:g.42690083T= , CM000668.1:g.42690083T= GRCh37
NC_000006.10:g.42798061T= NCBI36
NG_009176.1:g.5276A=
NG_009176.2:g.5276A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.-11A= MANE Select ENSP00000230381.5:n.-11A=
ENST00000230381.6:c.-11A= ENSP00000230381.5:n.-11A=
NM_000322.4:c.-11A= NP_000313.2:n.-11A=
XR_427834.2:n.645A=
XR_926295.1:n.645A=
XR_427834.4:n.695A=
XR_926295.3:n.695A=
NM_000322.5:c.-11A= MANE Select NP_000313.2:n.-11A=