Canonical Allele Identifier: CA374864274

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123370950C>G , CM000671.2:g.123370950C>G	GRCh38
NC_000009.11:g.126133229C>G , CM000671.1:g.126133229C>G	GRCh37
NC_000009.10:g.125173050C>G	NCBI36
NG_051311.1:g.21886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.1897C>G MANE Select	ENSP00000362734.3:p.Arg633Gly
ENST00000359999.7:c.1897C>G	ENSP00000353092.3:p.Arg633Gly
ENST00000373631.7:c.1897C>G	ENSP00000362734.3:p.Arg633Gly
ENST00000460253.1:c.901C>G	ENSP00000435279.1:p.Arg301Gly
NM_173689.6:c.1897C>G	NP_775960.4:p.Arg633Gly
NR_104603.1:n.1011C>G
XM_005251934.1:c.901C>G	XP_005251991.1:p.Arg301Gly
XM_011518556.1:c.1897C>G	XP_011516858.1:p.Arg633Gly
XM_011518557.1:c.1702C>G	XP_011516859.1:p.Arg568Gly
XM_011518558.1:c.1702C>G	XP_011516860.1:p.Arg568Gly
XM_005251934.3:c.901C>G	XP_005251991.1:p.Arg301Gly
XM_011518556.3:c.1897C>G	XP_011516858.1:p.Arg633Gly
XM_011518557.3:c.1702C>G	XP_011516859.1:p.Arg568Gly
XM_011518558.3:c.1702C>G	XP_011516860.1:p.Arg568Gly
NM_173689.7:c.1897C>G MANE Select	NP_775960.4:p.Arg633Gly
NR_104603.2:n.1011C>G