Canonical Allele Identifier: CA2558449061
Gene: PRPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722335G>A , CM000668.2:g.42722335G>A GRCh38
NC_000006.11:g.42690073G>A , CM000668.1:g.42690073G>A GRCh37
NC_000006.10:g.42798051G>A NCBI36
NG_009176.1:g.5286C>T
NG_009176.2:g.5286C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.-1C>T MANE Select ENSP00000230381.5:n.-1C>T
ENST00000230381.6:c.-1C>T ENSP00000230381.5:n.-1C>T
NM_000322.4:c.-1C>T NP_000313.2:n.-1C>T
XR_427834.2:n.655C>T
XR_926295.1:n.655C>T
XR_427834.4:n.705C>T
XR_926295.3:n.705C>T
NM_000322.5:c.-1C>T MANE Select NP_000313.2:n.-1C>T