Canonical Allele Identifier: CA364137531
Gene: PRPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.42689622A>G (hg19) chr6:g.42721884A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721884A>G , CM000668.2:g.42721884A>G GRCh38
NC_000006.11:g.42689622A>G , CM000668.1:g.42689622A>G GRCh37
NC_000006.10:g.42797600A>G NCBI36
NG_009176.1:g.5737T>C
NG_009176.2:g.5737T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000230381.7:c.451T>C MANE Select ENSP00000230381.5:p.Phe151Leu
ENST00000230381.6:c.451T>C ENSP00000230381.5:p.Phe151Leu
NM_000322.4:c.451T>C NP_000313.2:p.Phe151Leu
XR_427834.2:n.1106T>C
XR_926295.1:n.1106T>C
XR_427834.4:n.1156T>C
XR_926295.3:n.1156T>C
NM_000322.5:c.451T>C MANE Select NP_000313.2:p.Phe151Leu
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