Canonical Allele Identifier: CA859794858

Gene: CRB2

Linked Data

• dbSNP Id: rs1473812512
• gnomAD v4: 9-123377112-C-T
• MyVariant Identifiers: chr9:g.126139391C>T (hg19) ; chr9:g.123377112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377112C>T , CM000671.2:g.123377112C>T	GRCh38
NC_000009.11:g.126139391C>T , CM000671.1:g.126139391C>T	GRCh37
NC_000009.10:g.125179212C>T	NCBI36
NG_051311.1:g.28048C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*50C>T MANE Select	ENSP00000362734.3:n.*50C>T
ENST00000373631.7:c.*50C>T	ENSP00000362734.3:n.*50C>T
ENST00000460253.1:c.*50C>T	ENSP00000435279.1:n.*50C>T
NM_173689.6:c.*50C>T	NP_775960.4:n.*50C>T
NR_104603.1:n.3022C>T
XM_005251934.1:c.*50C>T	XP_005251991.1:n.*50C>T
XM_011518556.1:c.*50C>T	XP_011516858.1:n.*50C>T
XM_011518557.1:c.*50C>T	XP_011516859.1:n.*50C>T
XM_011518558.1:c.*50C>T	XP_011516860.1:n.*50C>T
XM_005251934.3:c.*50C>T	XP_005251991.1:n.*50C>T
XM_011518556.3:c.*50C>T	XP_011516858.1:n.*50C>T
XM_011518557.3:c.*50C>T	XP_011516859.1:n.*50C>T
XM_011518558.3:c.*50C>T	XP_011516860.1:n.*50C>T
NM_173689.7:c.*50C>T MANE Select	NP_775960.4:n.*50C>T
NR_104603.2:n.3022C>T