Canonical Allele Identifier: CA374869811

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139268A>T (hg19) ; chr9:g.123376989A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376989A>T , CM000671.2:g.123376989A>T	GRCh38
NC_000009.11:g.126139268A>T , CM000671.1:g.126139268A>T	GRCh37
NC_000009.10:g.125179089A>T	NCBI36
NG_051311.1:g.27925A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3785A>T MANE Select	ENSP00000362734.3:p.Gln1262Leu
ENST00000373631.7:c.3785A>T	ENSP00000362734.3:p.Gln1262Leu
ENST00000460253.1:c.2789A>T	ENSP00000435279.1:p.Gln930Leu
NM_173689.6:c.3785A>T	NP_775960.4:p.Gln1262Leu
NR_104603.1:n.2899A>T
XM_005251934.1:c.2789A>T	XP_005251991.1:p.Gln930Leu
XM_011518556.1:c.3758A>T	XP_011516858.1:p.Gln1253Leu
XM_011518557.1:c.3590A>T	XP_011516859.1:p.Gln1197Leu
XM_011518558.1:c.3590A>T	XP_011516860.1:p.Gln1197Leu
XM_005251934.3:c.2789A>T	XP_005251991.1:p.Gln930Leu
XM_011518556.3:c.3758A>T	XP_011516858.1:p.Gln1253Leu
XM_011518557.3:c.3590A>T	XP_011516859.1:p.Gln1197Leu
XM_011518558.3:c.3590A>T	XP_011516860.1:p.Gln1197Leu
NM_173689.7:c.3785A>T MANE Select	NP_775960.4:p.Gln1262Leu
NR_104603.2:n.2899A>T