Canonical Allele Identifier: CA467206755

Gene: CRB2

Linked Data

• gnomAD v4: 9-123373801-C-G
• MyVariant Identifiers: chr9:g.126136080C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123373801C>G , CM000671.2:g.123373801C>G	GRCh38
NC_000009.11:g.126136080C>G , CM000671.1:g.126136080C>G	GRCh37
NC_000009.10:g.125175901C>G	NCBI36
NG_051311.1:g.24737C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3270C>G MANE Select	ENSP00000362734.3:p.Arg1090=
ENST00000359999.7:c.3270C>G	ENSP00000353092.3:p.Arg1090=
ENST00000373631.7:c.3270C>G	ENSP00000362734.3:p.Arg1090=
ENST00000460253.1:c.2274C>G	ENSP00000435279.1:p.Arg758=
NM_173689.6:c.3270C>G	NP_775960.4:p.Arg1090=
NR_104603.1:n.2384C>G
XM_005251934.1:c.2274C>G	XP_005251991.1:p.Arg758=
XM_011518556.1:c.3243C>G	XP_011516858.1:p.Arg1081=
XM_011518557.1:c.3075C>G	XP_011516859.1:p.Arg1025=
XM_011518558.1:c.3075C>G	XP_011516860.1:p.Arg1025=
XM_005251934.3:c.2274C>G	XP_005251991.1:p.Arg758=
XM_011518556.3:c.3243C>G	XP_011516858.1:p.Arg1081=
XM_011518557.3:c.3075C>G	XP_011516859.1:p.Arg1025=
XM_011518558.3:c.3075C>G	XP_011516860.1:p.Arg1025=
NM_173689.7:c.3270C>G MANE Select	NP_775960.4:p.Arg1090=
NR_104603.2:n.2384C>G