Canonical Allele Identifier: CA156253972

Gene: RP9

Linked Data

• dbSNP Id: rs1030399062
• MyVariant Identifiers: chr7:g.33136000G>A (hg19) ; chr7:g.33096388G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096388G>A , CM000669.2:g.33096388G>A	GRCh38
NC_000007.13:g.33136000G>A , CM000669.1:g.33136000G>A	GRCh37
NC_000007.12:g.33102525G>A	NCBI36
NG_012968.1:g.18003C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2440+105C>T
ENST00000492391.2:n.1591+105C>T
ENST00000682645.1:n.3538+105C>T
ENST00000683432.1:c.*642+105C>T	ENSP00000508174.1:n.*642+105C>T
ENST00000684207.1:c.*101C>T	ENSP00000506942.1:n.*101C>T
ENST00000297157.8:c.467+105C>T MANE Select	ENSP00000297157.3:n.467+105C>T
ENST00000297157.7:c.467+105C>T	ENSP00000297157.3:n.467+105C>T
ENST00000448915.1:c.365+105C>T	ENSP00000411577.1:n.365+105C>T
NM_203288.1:c.467+105C>T	NP_976033.1:n.467+105C>T
XM_011515468.1:c.365+105C>T	XP_011513770.1:n.365+105C>T
XM_011515468.3:c.365+105C>T	XP_011513770.1:n.365+105C>T
NM_203288.2:c.467+105C>T MANE Select	NP_976033.1:n.467+105C>T