Canonical Allele Identifier: CA1624187218

Gene: PRPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42722355G= , CM000668.2:g.42722355G=	GRCh38
NC_000006.11:g.42690093G= , CM000668.1:g.42690093G=	GRCh37
NC_000006.10:g.42798071G=	NCBI36
NG_009176.1:g.5266C=
NG_009176.2:g.5266C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.-21C= MANE Select	ENSP00000230381.5:n.-21C=
ENST00000230381.6:c.-21C=	ENSP00000230381.5:n.-21C=
NM_000322.4:c.-21C=	NP_000313.2:n.-21C=
XR_427834.2:n.635C=
XR_926295.1:n.635C=
XR_427834.4:n.685C=
XR_926295.3:n.685C=
NM_000322.5:c.-21C= MANE Select	NP_000313.2:n.-21C=