Canonical Allele Identifier: CA364138816
Gene: PRPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.42689996A>G (hg19) chr6:g.42722258A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722258A>G , CM000668.2:g.42722258A>G GRCh38
NC_000006.11:g.42689996A>G , CM000668.1:g.42689996A>G GRCh37
NC_000006.10:g.42797974A>G NCBI36
NG_009176.1:g.5363T>C
NG_009176.2:g.5363T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.77T>C MANE Select ENSP00000230381.5:p.Phe26Ser
ENST00000230381.6:c.77T>C ENSP00000230381.5:p.Phe26Ser
NM_000322.4:c.77T>C NP_000313.2:p.Phe26Ser
XR_427834.2:n.732T>C
XR_926295.1:n.732T>C
XR_427834.4:n.782T>C
XR_926295.3:n.782T>C
NM_000322.5:c.77T>C MANE Select NP_000313.2:p.Phe26Ser
Search 100 bp 5'
Search 100 bp 3'