Canonical Allele Identifier: CA467090860

Gene: CRB2

Linked Data

• gnomAD v4: 9-123377002-T-G
• MyVariant Identifiers: chr9:g.126139281T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377002T>G , CM000671.2:g.123377002T>G	GRCh38
NC_000009.11:g.126139281T>G , CM000671.1:g.126139281T>G	GRCh37
NC_000009.10:g.125179102T>G	NCBI36
NG_051311.1:g.27938T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3798T>G MANE Select	ENSP00000362734.3:p.Ala1266=
ENST00000373631.7:c.3798T>G	ENSP00000362734.3:p.Ala1266=
ENST00000460253.1:c.2802T>G	ENSP00000435279.1:p.Ala934=
NM_173689.6:c.3798T>G	NP_775960.4:p.Ala1266=
NR_104603.1:n.2912T>G
XM_005251934.1:c.2802T>G	XP_005251991.1:p.Ala934=
XM_011518556.1:c.3771T>G	XP_011516858.1:p.Ala1257=
XM_011518557.1:c.3603T>G	XP_011516859.1:p.Ala1201=
XM_011518558.1:c.3603T>G	XP_011516860.1:p.Ala1201=
XM_005251934.3:c.2802T>G	XP_005251991.1:p.Ala934=
XM_011518556.3:c.3771T>G	XP_011516858.1:p.Ala1257=
XM_011518557.3:c.3603T>G	XP_011516859.1:p.Ala1201=
XM_011518558.3:c.3603T>G	XP_011516860.1:p.Ala1201=
NM_173689.7:c.3798T>G MANE Select	NP_775960.4:p.Ala1266=
NR_104603.2:n.2912T>G