Canonical Allele Identifier: CA374869882

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139300G>T (hg19) ; chr9:g.123377021G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377021G>T , CM000671.2:g.123377021G>T	GRCh38
NC_000009.11:g.126139300G>T , CM000671.1:g.126139300G>T	GRCh37
NC_000009.10:g.125179121G>T	NCBI36
NG_051311.1:g.27957G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3817G>T MANE Select	ENSP00000362734.3:p.Asp1273Tyr
ENST00000373631.7:c.3817G>T	ENSP00000362734.3:p.Asp1273Tyr
ENST00000460253.1:c.2821G>T	ENSP00000435279.1:p.Asp941Tyr
NM_173689.6:c.3817G>T	NP_775960.4:p.Asp1273Tyr
NR_104603.1:n.2931G>T
XM_005251934.1:c.2821G>T	XP_005251991.1:p.Asp941Tyr
XM_011518556.1:c.3790G>T	XP_011516858.1:p.Asp1264Tyr
XM_011518557.1:c.3622G>T	XP_011516859.1:p.Asp1208Tyr
XM_011518558.1:c.3622G>T	XP_011516860.1:p.Asp1208Tyr
XM_005251934.3:c.2821G>T	XP_005251991.1:p.Asp941Tyr
XM_011518556.3:c.3790G>T	XP_011516858.1:p.Asp1264Tyr
XM_011518557.3:c.3622G>T	XP_011516859.1:p.Asp1208Tyr
XM_011518558.3:c.3622G>T	XP_011516860.1:p.Asp1208Tyr
NM_173689.7:c.3817G>T MANE Select	NP_775960.4:p.Asp1273Tyr
NR_104603.2:n.2931G>T