Canonical Allele Identifier: CA2682311882
Gene: RP9 HGNC NCBI

Linked Data

gnomAD v4: 7-33096569-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096569A>G , CM000669.2:g.33096569A>G GRCh38
NC_000007.13:g.33136181A>G , CM000669.1:g.33136181A>G GRCh37
NC_000007.12:g.33102706A>G NCBI36
NG_012968.1:g.17822T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2379-15T>C
ENST00000492391.2:n.1530-15T>C
ENST00000682645.1:n.3477-15T>C
ENST00000683432.1:c.*581-15T>C ENSP00000508174.1:n.*581-15T>C
ENST00000684207.1:c.406-15T>C ENSP00000506942.1:n.406-15T>C
ENST00000297157.8:c.406-15T>C MANE Select ENSP00000297157.3:n.406-15T>C
ENST00000297157.7:c.406-15T>C ENSP00000297157.3:n.406-15T>C
ENST00000448915.1:c.304-15T>C ENSP00000411577.1:n.304-15T>C
NM_203288.1:c.406-15T>C NP_976033.1:n.406-15T>C
XM_011515468.1:c.304-15T>C XP_011513770.1:n.304-15T>C
XM_011515468.3:c.304-15T>C XP_011513770.1:n.304-15T>C
NM_203288.2:c.406-15T>C MANE Select NP_976033.1:n.406-15T>C
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