Canonical Allele Identifier: CA374869772

Gene: CRB2

Linked Data

• dbSNP Id: rs2042112708
• gnomAD v4: 9-123376971-G-T
• MyVariant Identifiers: chr9:g.126139250G>T (hg19) ; chr9:g.123376971G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376971G>T , CM000671.2:g.123376971G>T	GRCh38
NC_000009.11:g.126139250G>T , CM000671.1:g.126139250G>T	GRCh37
NC_000009.10:g.125179071G>T	NCBI36
NG_051311.1:g.27907G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3767G>T MANE Select	ENSP00000362734.3:p.Gly1256Val
ENST00000373631.7:c.3767G>T	ENSP00000362734.3:p.Gly1256Val
ENST00000460253.1:c.2771G>T	ENSP00000435279.1:p.Gly924Val
NM_173689.6:c.3767G>T	NP_775960.4:p.Gly1256Val
NR_104603.1:n.2881G>T
XM_005251934.1:c.2771G>T	XP_005251991.1:p.Gly924Val
XM_011518556.1:c.3740G>T	XP_011516858.1:p.Gly1247Val
XM_011518557.1:c.3572G>T	XP_011516859.1:p.Gly1191Val
XM_011518558.1:c.3572G>T	XP_011516860.1:p.Gly1191Val
XM_005251934.3:c.2771G>T	XP_005251991.1:p.Gly924Val
XM_011518556.3:c.3740G>T	XP_011516858.1:p.Gly1247Val
XM_011518557.3:c.3572G>T	XP_011516859.1:p.Gly1191Val
XM_011518558.3:c.3572G>T	XP_011516860.1:p.Gly1191Val
NM_173689.7:c.3767G>T MANE Select	NP_775960.4:p.Gly1256Val
NR_104603.2:n.2881G>T