Canonical Allele Identifier: CA138186821
Gene: PRPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1017652031
gnomAD v3: 6-42721549-T-C
gnomAD v4: 6-42721549-T-C
MyVariant Identifiers: chr6:g.42689287T>C (hg19) chr6:g.42721549T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42721549T>C , CM000668.2:g.42721549T>C GRCh38
NC_000006.11:g.42689287T>C , CM000668.1:g.42689287T>C GRCh37
NC_000006.10:g.42797265T>C NCBI36
NG_009176.1:g.6072A>G
NG_009176.2:g.6072A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000230381.7:c.581+205A>G MANE Select ENSP00000230381.5:n.581+205A>G
ENST00000230381.6:c.581+205A>G ENSP00000230381.5:n.581+205A>G
NM_000322.4:c.581+205A>G NP_000313.2:n.581+205A>G
XR_427834.2:n.1236+205A>G
XR_926295.1:n.1236+205A>G
XR_427834.4:n.1286+205A>G
XR_926295.3:n.1286+205A>G
NM_000322.5:c.581+205A>G MANE Select NP_000313.2:n.581+205A>G
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