Canonical Allele Identifier: CA374869918

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139316T>G (hg19) ; chr9:g.123377037T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377037T>G , CM000671.2:g.123377037T>G	GRCh38
NC_000009.11:g.126139316T>G , CM000671.1:g.126139316T>G	GRCh37
NC_000009.10:g.125179137T>G	NCBI36
NG_051311.1:g.27973T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3833T>G MANE Select	ENSP00000362734.3:p.Val1278Gly
ENST00000373631.7:c.3833T>G	ENSP00000362734.3:p.Val1278Gly
ENST00000460253.1:c.2837T>G	ENSP00000435279.1:p.Val946Gly
NM_173689.6:c.3833T>G	NP_775960.4:p.Val1278Gly
NR_104603.1:n.2947T>G
XM_005251934.1:c.2837T>G	XP_005251991.1:p.Val946Gly
XM_011518556.1:c.3806T>G	XP_011516858.1:p.Val1269Gly
XM_011518557.1:c.3638T>G	XP_011516859.1:p.Val1213Gly
XM_011518558.1:c.3638T>G	XP_011516860.1:p.Val1213Gly
XM_005251934.3:c.2837T>G	XP_005251991.1:p.Val946Gly
XM_011518556.3:c.3806T>G	XP_011516858.1:p.Val1269Gly
XM_011518557.3:c.3638T>G	XP_011516859.1:p.Val1213Gly
XM_011518558.3:c.3638T>G	XP_011516860.1:p.Val1213Gly
NM_173689.7:c.3833T>G MANE Select	NP_775960.4:p.Val1278Gly
NR_104603.2:n.2947T>G