Canonical Allele Identifier: CA364138458
Gene: PRPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722145A>T , CM000668.2:g.42722145A>T GRCh38
NC_000006.11:g.42689883A>T , CM000668.1:g.42689883A>T GRCh37
NC_000006.10:g.42797861A>T NCBI36
NG_009176.1:g.5476T>A
NG_009176.2:g.5476T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.190T>A MANE Select ENSP00000230381.5:p.Leu64Met
ENST00000230381.6:c.190T>A ENSP00000230381.5:p.Leu64Met
NM_000322.4:c.190T>A NP_000313.2:p.Leu64Met
XR_427834.2:n.845T>A
XR_926295.1:n.845T>A
XR_427834.4:n.895T>A
XR_926295.3:n.895T>A
NM_000322.5:c.190T>A MANE Select NP_000313.2:p.Leu64Met