Canonical Allele Identifier: CA374869851

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139285G>T (hg19) ; chr9:g.123377006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377006G>T , CM000671.2:g.123377006G>T	GRCh38
NC_000009.11:g.126139285G>T , CM000671.1:g.126139285G>T	GRCh37
NC_000009.10:g.125179106G>T	NCBI36
NG_051311.1:g.27942G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3802G>T MANE Select	ENSP00000362734.3:p.Ala1268Ser
ENST00000373631.7:c.3802G>T	ENSP00000362734.3:p.Ala1268Ser
ENST00000460253.1:c.2806G>T	ENSP00000435279.1:p.Ala936Ser
NM_173689.6:c.3802G>T	NP_775960.4:p.Ala1268Ser
NR_104603.1:n.2916G>T
XM_005251934.1:c.2806G>T	XP_005251991.1:p.Ala936Ser
XM_011518556.1:c.3775G>T	XP_011516858.1:p.Ala1259Ser
XM_011518557.1:c.3607G>T	XP_011516859.1:p.Ala1203Ser
XM_011518558.1:c.3607G>T	XP_011516860.1:p.Ala1203Ser
XM_005251934.3:c.2806G>T	XP_005251991.1:p.Ala936Ser
XM_011518556.3:c.3775G>T	XP_011516858.1:p.Ala1259Ser
XM_011518557.3:c.3607G>T	XP_011516859.1:p.Ala1203Ser
XM_011518558.3:c.3607G>T	XP_011516860.1:p.Ala1203Ser
NM_173689.7:c.3802G>T MANE Select	NP_775960.4:p.Ala1268Ser
NR_104603.2:n.2916G>T