Canonical Allele Identifier: CA364138511
Gene: PRPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722156A>T , CM000668.2:g.42722156A>T GRCh38
NC_000006.11:g.42689894A>T , CM000668.1:g.42689894A>T GRCh37
NC_000006.10:g.42797872A>T NCBI36
NG_009176.1:g.5465T>A
NG_009176.2:g.5465T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.179T>A MANE Select ENSP00000230381.5:p.Val60Glu
ENST00000230381.6:c.179T>A ENSP00000230381.5:p.Val60Glu
NM_000322.4:c.179T>A NP_000313.2:p.Val60Glu
XR_427834.2:n.834T>A
XR_926295.1:n.834T>A
XR_427834.4:n.884T>A
XR_926295.3:n.884T>A
NM_000322.5:c.179T>A MANE Select NP_000313.2:p.Val60Glu