Canonical Allele Identifier: CA364138557
Gene: PRPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722163G>C , CM000668.2:g.42722163G>C GRCh38
NC_000006.11:g.42689901G>C , CM000668.1:g.42689901G>C GRCh37
NC_000006.10:g.42797879G>C NCBI36
NG_009176.1:g.5458C>G
NG_009176.2:g.5458C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.172C>G MANE Select ENSP00000230381.5:p.His58Asp
ENST00000230381.6:c.172C>G ENSP00000230381.5:p.His58Asp
NM_000322.4:c.172C>G NP_000313.2:p.His58Asp
XR_427834.2:n.827C>G
XR_926295.1:n.827C>G
XR_427834.4:n.877C>G
XR_926295.3:n.877C>G
NM_000322.5:c.172C>G MANE Select NP_000313.2:p.His58Asp