Canonical Allele Identifier: CA199643118

Gene: CRB2

Linked Data

• dbSNP Id: rs752532866
• gnomAD v2: 9-126139320-A-G
• gnomAD v3: 9-123377041-A-G
• gnomAD v4: 9-123377041-A-G
• MyVariant Identifiers: chr9:g.126139320A>G (hg19) ; chr9:g.123377041A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377041A>G , CM000671.2:g.123377041A>G	GRCh38
NC_000009.11:g.126139320A>G , CM000671.1:g.126139320A>G	GRCh37
NC_000009.10:g.125179141A>G	NCBI36
NG_051311.1:g.27977A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3837A>G MANE Select	ENSP00000362734.3:p.Pro1279=
ENST00000373631.7:c.3837A>G	ENSP00000362734.3:p.Pro1279=
ENST00000460253.1:c.2841A>G	ENSP00000435279.1:p.Pro947=
NM_173689.6:c.3837A>G	NP_775960.4:p.Pro1279=
NR_104603.1:n.2951A>G
XM_005251934.1:c.2841A>G	XP_005251991.1:p.Pro947=
XM_011518556.1:c.3810A>G	XP_011516858.1:p.Pro1270=
XM_011518557.1:c.3642A>G	XP_011516859.1:p.Pro1214=
XM_011518558.1:c.3642A>G	XP_011516860.1:p.Pro1214=
XM_005251934.3:c.2841A>G	XP_005251991.1:p.Pro947=
XM_011518556.3:c.3810A>G	XP_011516858.1:p.Pro1270=
XM_011518557.3:c.3642A>G	XP_011516859.1:p.Pro1214=
XM_011518558.3:c.3642A>G	XP_011516860.1:p.Pro1214=
NM_173689.7:c.3837A>G MANE Select	NP_775960.4:p.Pro1279=
NR_104603.2:n.2951A>G