Canonical Allele Identifier: CA573515759

Gene: RP9

Linked Data

• dbSNP Id: rs1460110879
• gnomAD v2: 7-33136070-T-C
• gnomAD v4: 7-33096458-T-C
• MyVariant Identifiers: chr7:g.33136070T>C (hg19) ; chr7:g.33096458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096458T>C , CM000669.2:g.33096458T>C	GRCh38
NC_000007.13:g.33136070T>C , CM000669.1:g.33136070T>C	GRCh37
NC_000007.12:g.33102595T>C	NCBI36
NG_012968.1:g.17933A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2440+35A>G
ENST00000492391.2:n.1591+35A>G
ENST00000682645.1:n.3538+35A>G
ENST00000683432.1:c.*642+35A>G	ENSP00000508174.1:n.*642+35A>G
ENST00000684207.1:c.*31A>G	ENSP00000506942.1:n.*31A>G
ENST00000297157.8:c.467+35A>G MANE Select	ENSP00000297157.3:n.467+35A>G
ENST00000297157.7:c.467+35A>G	ENSP00000297157.3:n.467+35A>G
ENST00000448915.1:c.365+35A>G	ENSP00000411577.1:n.365+35A>G
NM_203288.1:c.467+35A>G	NP_976033.1:n.467+35A>G
XM_011515468.1:c.365+35A>G	XP_011513770.1:n.365+35A>G
XM_011515468.3:c.365+35A>G	XP_011513770.1:n.365+35A>G
NM_203288.2:c.467+35A>G MANE Select	NP_976033.1:n.467+35A>G