Canonical Allele Identifier: CA374869935

Gene: CRB2

Linked Data

• gnomAD v4: 9-123377047-G-C
• MyVariant Identifiers: chr9:g.126139326G>C (hg19) ; chr9:g.123377047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377047G>C , CM000671.2:g.123377047G>C	GRCh38
NC_000009.11:g.126139326G>C , CM000671.1:g.126139326G>C	GRCh37
NC_000009.10:g.125179147G>C	NCBI36
NG_051311.1:g.27983G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3843G>C MANE Select	ENSP00000362734.3:p.Glu1281Asp
ENST00000373631.7:c.3843G>C	ENSP00000362734.3:p.Glu1281Asp
ENST00000460253.1:c.2847G>C	ENSP00000435279.1:p.Glu949Asp
NM_173689.6:c.3843G>C	NP_775960.4:p.Glu1281Asp
NR_104603.1:n.2957G>C
XM_005251934.1:c.2847G>C	XP_005251991.1:p.Glu949Asp
XM_011518556.1:c.3816G>C	XP_011516858.1:p.Glu1272Asp
XM_011518557.1:c.3648G>C	XP_011516859.1:p.Glu1216Asp
XM_011518558.1:c.3648G>C	XP_011516860.1:p.Glu1216Asp
XM_005251934.3:c.2847G>C	XP_005251991.1:p.Glu949Asp
XM_011518556.3:c.3816G>C	XP_011516858.1:p.Glu1272Asp
XM_011518557.3:c.3648G>C	XP_011516859.1:p.Glu1216Asp
XM_011518558.3:c.3648G>C	XP_011516860.1:p.Glu1216Asp
NM_173689.7:c.3843G>C MANE Select	NP_775960.4:p.Glu1281Asp
NR_104603.2:n.2957G>C