Canonical Allele Identifier: CA1624170711
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42704611A= , CM000668.2:g.42704611A= GRCh38
NC_000006.11:g.42672349A= , CM000668.1:g.42672349A= GRCh37
NC_000006.10:g.42780327A= NCBI36
NG_009176.1:g.23010T=
NG_009176.2:g.23010T=

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.582T= MANE Select ENSP00000230381.5:p.Asp194=
ENST00000230381.6:c.582T= ENSP00000230381.5:p.Asp194=
NM_000322.4:c.582T= NP_000313.2:p.Asp194=
XR_427834.2:n.1237T=
XR_926295.1:n.1419T=
XR_427834.4:n.1287T=
XR_926295.3:n.1469T=
NM_000322.5:c.582T= MANE Select NP_000313.2:p.Asp194=