Canonical Allele Identifier: CA1624187211
Gene: PRPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42722347T= , CM000668.2:g.42722347T= GRCh38
NC_000006.11:g.42690085T= , CM000668.1:g.42690085T= GRCh37
NC_000006.10:g.42798063T= NCBI36
NG_009176.1:g.5274A=
NG_009176.2:g.5274A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.-13A= MANE Select ENSP00000230381.5:n.-13A=
ENST00000230381.6:c.-13A= ENSP00000230381.5:n.-13A=
NM_000322.4:c.-13A= NP_000313.2:n.-13A=
XR_427834.2:n.643A=
XR_926295.1:n.643A=
XR_427834.4:n.693A=
XR_926295.3:n.693A=
NM_000322.5:c.-13A= MANE Select NP_000313.2:n.-13A=
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