Canonical Allele Identifier: CA422808925

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1933048
• ClinVar RCV Id: RCV002635741
• dbSNP Id: rs1346978684
• gnomAD v2: 1-197397020-A-G
• gnomAD v4: 1-197427890-A-G
• MyVariant Identifiers: chr1:g.197397020A>G (hg19) ; chr1:g.197427890A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427890A>G , CM000663.2:g.197427890A>G	GRCh38
NC_000001.10:g.197397020A>G , CM000663.1:g.197397020A>G	GRCh37
NC_000001.9:g.195663643A>G	NCBI36
NG_008483.1:g.164613A>G
NG_008483.2:g.231429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2565A>G MANE Select	ENSP00000356370.3:p.Val855=
ENST00000638467.1:c.2565A>G	ENSP00000491102.1:p.Val855=
ENST00000681519.1:c.1446A>G	ENSP00000505267.1:p.Val482=
ENST00000367397.1:c.708A>G	ENSP00000356367.1:p.Val236=
ENST00000367399.6:c.2229A>G	ENSP00000356369.2:p.Val743=
ENST00000367400.7:c.2565A>G	ENSP00000356370.3:p.Val855=
ENST00000484075.5:c.2565A>G	ENSP00000433932.1:p.Val855=
ENST00000535699.5:c.2358A>G	ENSP00000438786.1:p.Val786=
ENST00000538660.5:c.2128+5934A>G	ENSP00000438091.1:n.2128+5934A>G
NM_001193640.1:c.2229A>G	NP_001180569.1:p.Val743=
NM_001257965.1:c.2358A>G	NP_001244894.1:p.Val786=
NM_001257966.1:c.2128+5934A>G	NP_001244895.1:n.2128+5934A>G
NM_201253.2:c.2565A>G	NP_957705.1:p.Val855=
NR_047563.1:n.2566A>G
NR_047564.1:n.2774A>G
XM_011509365.1:c.2565A>G	XP_011507667.1:p.Val855=
XM_011509366.1:c.2565A>G	XP_011507668.1:p.Val855=
XM_011509367.1:c.2565A>G	XP_011507669.1:p.Val855=
XM_011509368.1:c.1983A>G	XP_011507670.1:p.Val661=
XM_011509369.1:c.1008A>G	XP_011507671.1:p.Val336=
XM_011509365.2:c.2565A>G	XP_011507667.1:p.Val855=
XM_011509369.2:c.1008A>G	XP_011507671.1:p.Val336=
XM_017000851.1:c.1722A>G	XP_016856340.1:p.Val574=
XM_017000852.1:c.2565A>G	XP_016856341.1:p.Val855=
NM_201253.3:c.2565A>G MANE Select	NP_957705.1:p.Val855=
NM_001193640.2:c.2229A>G	NP_001180569.1:p.Val743=
NM_001257965.2:c.2358A>G	NP_001244894.1:p.Val786=
NR_047563.2:n.2518A>G
NR_047564.2:n.2726A>G
NM_001257966.2:c.2128+5934A>G	NP_001244895.1:n.2128+5934A>G