Canonical Allele Identifier: CA367181678
Gene: RP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096556T>A , CM000669.2:g.33096556T>A GRCh38
NC_000007.13:g.33136168T>A , CM000669.1:g.33136168T>A GRCh37
NC_000007.12:g.33102693T>A NCBI36
NG_012968.1:g.17835A>T

Transcript Alleles

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