Canonical Allele Identifier: CA1624187227

Gene: PRPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42722376C= , CM000668.2:g.42722376C=	GRCh38
NC_000006.11:g.42690114C= , CM000668.1:g.42690114C=	GRCh37
NC_000006.10:g.42798092C=	NCBI36
NG_009176.1:g.5245G=
NG_009176.2:g.5245G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.-42G= MANE Select	ENSP00000230381.5:n.-42G=
ENST00000230381.6:c.-42G=	ENSP00000230381.5:n.-42G=
NM_000322.4:c.-42G=	NP_000313.2:n.-42G=
XR_427834.2:n.614G=
XR_926295.1:n.614G=
XR_427834.4:n.664G=
XR_926295.3:n.664G=
NM_000322.5:c.-42G= MANE Select	NP_000313.2:n.-42G=