Canonical Allele Identifier: CA364138141
Gene: PRPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722087T>G , CM000668.2:g.42722087T>G GRCh38
NC_000006.11:g.42689825T>G , CM000668.1:g.42689825T>G GRCh37
NC_000006.10:g.42797803T>G NCBI36
NG_009176.1:g.5534A>C
NG_009176.2:g.5534A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.248A>C MANE Select ENSP00000230381.5:p.Tyr83Ser
ENST00000230381.6:c.248A>C ENSP00000230381.5:p.Tyr83Ser
NM_000322.4:c.248A>C NP_000313.2:p.Tyr83Ser
XR_427834.2:n.903A>C
XR_926295.1:n.903A>C
XR_427834.4:n.953A>C
XR_926295.3:n.953A>C
NM_000322.5:c.248A>C MANE Select NP_000313.2:p.Tyr83Ser