Canonical Allele Identifier: CA1624186978

Gene: PRPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42721835C= , CM000668.2:g.42721835C=	GRCh38
NC_000006.11:g.42689573C= , CM000668.1:g.42689573C=	GRCh37
NC_000006.10:g.42797551C=	NCBI36
NG_009176.1:g.5786G=
NG_009176.2:g.5786G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230381.7:c.500G= MANE Select	ENSP00000230381.5:p.Gly167=
ENST00000230381.6:c.500G=	ENSP00000230381.5:p.Gly167=
NM_000322.4:c.500G=	NP_000313.2:p.Gly167=
XR_427834.2:n.1155G=
XR_926295.1:n.1155G=
XR_427834.4:n.1205G=
XR_926295.3:n.1205G=
NM_000322.5:c.500G= MANE Select	NP_000313.2:p.Gly167=