Canonical Allele Identifier: CA227994
Gene: CRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99871
ClinVar RCV Id: RCV000086309
dbSNP Id: rs62636265

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421267G>A , CM000663.2:g.197421267G>A GRCh38
NC_000001.10:g.197390397G>A , CM000663.1:g.197390397G>A GRCh37
NC_000001.9:g.195657020G>A NCBI36
NG_008483.1:g.157990G>A
NG_008483.2:g.224806G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367400.8:c.1439G>A MANE Select ENSP00000356370.3:p.Cys480Tyr
ENST00000638467.1:c.1439G>A ENSP00000491102.1:p.Cys480Tyr
ENST00000681519.1:c.320G>A ENSP00000505267.1:p.Cys107Tyr
ENST00000367397.1:c.-419G>A ENSP00000356367.1:n.-419G>A
ENST00000367399.6:c.1103G>A ENSP00000356369.2:p.Cys368Tyr
ENST00000367400.7:c.1439G>A ENSP00000356370.3:p.Cys480Tyr
ENST00000476483.1:n.399G>A
ENST00000484075.5:c.1439G>A ENSP00000433932.1:p.Cys480Tyr
ENST00000535699.5:c.1232G>A ENSP00000438786.1:p.Cys411Tyr
ENST00000538660.5:c.1439G>A ENSP00000438091.1:p.Cys480Tyr
NM_001193640.1:c.1103G>A NP_001180569.1:p.Cys368Tyr
NM_001257965.1:c.1232G>A NP_001244894.1:p.Cys411Tyr
NM_001257966.1:c.1439G>A NP_001244895.1:p.Cys480Tyr
NM_201253.2:c.1439G>A NP_957705.1:p.Cys480Tyr
NR_047563.1:n.1648G>A
NR_047564.1:n.1648G>A
XM_011509365.1:c.1439G>A XP_011507667.1:p.Cys480Tyr
XM_011509366.1:c.1439G>A XP_011507668.1:p.Cys480Tyr
XM_011509367.1:c.1439G>A XP_011507669.1:p.Cys480Tyr
XM_011509368.1:c.857G>A XP_011507670.1:p.Cys286Tyr
XM_011509369.1:c.-119G>A XP_011507671.1:n.-119G>A
XM_011509365.2:c.1439G>A XP_011507667.1:p.Cys480Tyr
XM_011509369.2:c.-119G>A XP_011507671.1:n.-119G>A
XM_017000851.1:c.596G>A XP_016856340.1:p.Cys199Tyr
XM_017000852.1:c.1439G>A XP_016856341.1:p.Cys480Tyr
NM_201253.3:c.1439G>A MANE Select NP_957705.1:p.Cys480Tyr
NM_001193640.2:c.1103G>A NP_001180569.1:p.Cys368Tyr
NM_001257965.2:c.1232G>A NP_001244894.1:p.Cys411Tyr
NR_047563.2:n.1600G>A
NR_047564.2:n.1600G>A
NM_001257966.2:c.1439G>A NP_001244895.1:p.Cys480Tyr