Canonical Allele Identifier: CA450362564
Gene: PRPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1432621932
gnomAD v3: 6-42721996-G-A
gnomAD v4: 6-42721996-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721996G>A , CM000668.2:g.42721996G>A GRCh38
NC_000006.11:g.42689734G>A , CM000668.1:g.42689734G>A GRCh37
NC_000006.10:g.42797712G>A NCBI36
NG_009176.1:g.5625C>T
NG_009176.2:g.5625C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.339C>T MANE Select ENSP00000230381.5:p.Phe113=
ENST00000230381.6:c.339C>T ENSP00000230381.5:p.Phe113=
NM_000322.4:c.339C>T NP_000313.2:p.Phe113=
XR_427834.2:n.994C>T
XR_926295.1:n.994C>T
XR_427834.4:n.1044C>T
XR_926295.3:n.1044C>T
NM_000322.5:c.339C>T MANE Select NP_000313.2:p.Phe113=