Canonical Allele Identifier: CA422808335

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1609785
• ClinVar RCV Id: RCV002152682
• dbSNP Id: rs2125469375
• gnomAD v4: 1-197421190-A-G
• MyVariant Identifiers: chr1:g.197390320A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421190A>G , CM000663.2:g.197421190A>G	GRCh38
NC_000001.10:g.197390320A>G , CM000663.1:g.197390320A>G	GRCh37
NC_000001.9:g.195656943A>G	NCBI36
NG_008483.1:g.157913A>G
NG_008483.2:g.224729A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1362A>G MANE Select	ENSP00000356370.3:p.Gly454=
ENST00000638467.1:c.1362A>G	ENSP00000491102.1:p.Gly454=
ENST00000681519.1:c.243A>G	ENSP00000505267.1:p.Gly81=
ENST00000367397.1:c.-496A>G	ENSP00000356367.1:n.-496A>G
ENST00000367399.6:c.1026A>G	ENSP00000356369.2:p.Gly342=
ENST00000367400.7:c.1362A>G	ENSP00000356370.3:p.Gly454=
ENST00000476483.1:n.322A>G
ENST00000484075.5:c.1362A>G	ENSP00000433932.1:p.Gly454=
ENST00000535699.5:c.1155A>G	ENSP00000438786.1:p.Gly385=
ENST00000538660.5:c.1362A>G	ENSP00000438091.1:p.Gly454=
NM_001193640.1:c.1026A>G	NP_001180569.1:p.Gly342=
NM_001257965.1:c.1155A>G	NP_001244894.1:p.Gly385=
NM_001257966.1:c.1362A>G	NP_001244895.1:p.Gly454=
NM_201253.2:c.1362A>G	NP_957705.1:p.Gly454=
NR_047563.1:n.1571A>G
NR_047564.1:n.1571A>G
XM_011509365.1:c.1362A>G	XP_011507667.1:p.Gly454=
XM_011509366.1:c.1362A>G	XP_011507668.1:p.Gly454=
XM_011509367.1:c.1362A>G	XP_011507669.1:p.Gly454=
XM_011509368.1:c.780A>G	XP_011507670.1:p.Gly260=
XM_011509369.1:c.-196A>G	XP_011507671.1:n.-196A>G
XM_011509365.2:c.1362A>G	XP_011507667.1:p.Gly454=
XM_011509369.2:c.-196A>G	XP_011507671.1:n.-196A>G
XM_017000851.1:c.519A>G	XP_016856340.1:p.Gly173=
XM_017000852.1:c.1362A>G	XP_016856341.1:p.Gly454=
NM_201253.3:c.1362A>G MANE Select	NP_957705.1:p.Gly454=
NM_001193640.2:c.1026A>G	NP_001180569.1:p.Gly342=
NM_001257965.2:c.1155A>G	NP_001244894.1:p.Gly385=
NR_047563.2:n.1523A>G
NR_047564.2:n.1523A>G
NM_001257966.2:c.1362A>G	NP_001244895.1:p.Gly454=