Canonical Allele Identifier: CA422808637

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1532391
• ClinVar RCV Id: RCV002085011
• dbSNP Id: rs2125471484
• MyVariant Identifiers: chr1:g.197390878A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421748A>G , CM000663.2:g.197421748A>G	GRCh38
NC_000001.10:g.197390878A>G , CM000663.1:g.197390878A>G	GRCh37
NC_000001.9:g.195657501A>G	NCBI36
NG_008483.1:g.158471A>G
NG_008483.2:g.225287A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1920A>G MANE Select	ENSP00000356370.3:p.Val640=
ENST00000638467.1:c.1920A>G	ENSP00000491102.1:p.Val640=
ENST00000681519.1:c.801A>G	ENSP00000505267.1:p.Val267=
ENST00000367397.1:c.63A>G	ENSP00000356367.1:p.Val21=
ENST00000367399.6:c.1584A>G	ENSP00000356369.2:p.Val528=
ENST00000367400.7:c.1920A>G	ENSP00000356370.3:p.Val640=
ENST00000484075.5:c.1920A>G	ENSP00000433932.1:p.Val640=
ENST00000535699.5:c.1713A>G	ENSP00000438786.1:p.Val571=
ENST00000538660.5:c.1920A>G	ENSP00000438091.1:p.Val640=
NM_001193640.1:c.1584A>G	NP_001180569.1:p.Val528=
NM_001257965.1:c.1713A>G	NP_001244894.1:p.Val571=
NM_001257966.1:c.1920A>G	NP_001244895.1:p.Val640=
NM_201253.2:c.1920A>G	NP_957705.1:p.Val640=
NR_047563.1:n.1923-2A>G
NR_047564.1:n.2129A>G
XM_011509365.1:c.1920A>G	XP_011507667.1:p.Val640=
XM_011509366.1:c.1920A>G	XP_011507668.1:p.Val640=
XM_011509367.1:c.1920A>G	XP_011507669.1:p.Val640=
XM_011509368.1:c.1338A>G	XP_011507670.1:p.Val446=
XM_011509369.1:c.363A>G	XP_011507671.1:p.Val121=
XM_011509365.2:c.1920A>G	XP_011507667.1:p.Val640=
XM_011509369.2:c.363A>G	XP_011507671.1:p.Val121=
XM_017000851.1:c.1077A>G	XP_016856340.1:p.Val359=
XM_017000852.1:c.1920A>G	XP_016856341.1:p.Val640=
NM_201253.3:c.1920A>G MANE Select	NP_957705.1:p.Val640=
NM_001193640.2:c.1584A>G	NP_001180569.1:p.Val528=
NM_001257965.2:c.1713A>G	NP_001244894.1:p.Val571=
NR_047563.2:n.1875-2A>G
NR_047564.2:n.2081A>G
NM_001257966.2:c.1920A>G	NP_001244895.1:p.Val640=