Canonical Allele Identifier: CA467090857

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139281T>C (hg19)

Genomic Alleles

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

Transcript Alleles

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