Canonical Allele Identifier: CA2678772486
Gene: PRPH2 HGNC NCBI

Linked Data

gnomAD v4: 6-42721658-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721658A>T , CM000668.2:g.42721658A>T GRCh38
NC_000006.11:g.42689396A>T , CM000668.1:g.42689396A>T GRCh37
NC_000006.10:g.42797374A>T NCBI36
NG_009176.1:g.5963T>A
NG_009176.2:g.5963T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.581+96T>A MANE Select ENSP00000230381.5:n.581+96T>A
ENST00000230381.6:c.581+96T>A ENSP00000230381.5:n.581+96T>A
NM_000322.4:c.581+96T>A NP_000313.2:n.581+96T>A
XR_427834.2:n.1236+96T>A
XR_926295.1:n.1236+96T>A
XR_427834.4:n.1286+96T>A
XR_926295.3:n.1286+96T>A
NM_000322.5:c.581+96T>A MANE Select NP_000313.2:n.581+96T>A
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