Canonical Allele Identifier: CA35900696

Gene: CRB1

Linked Data

• dbSNP Id: rs150726045
• gnomAD v2: 1-197396787-A-T
• gnomAD v3: 1-197427657-A-T
• gnomAD v4: 1-197427657-A-T
• MyVariant Identifiers: chr1:g.197396787A>T (hg19) ; chr1:g.197427657A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427657A>T , CM000663.2:g.197427657A>T	GRCh38
NC_000001.10:g.197396787A>T , CM000663.1:g.197396787A>T	GRCh37
NC_000001.9:g.195663410A>T	NCBI36
NG_008483.1:g.164380A>T
NG_008483.2:g.231196A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2332A>T MANE Select	ENSP00000356370.3:p.Asn778Tyr
ENST00000638467.1:c.2332A>T	ENSP00000491102.1:p.Asn778Tyr
ENST00000681519.1:c.1213A>T	ENSP00000505267.1:p.Asn405Tyr
ENST00000367397.1:c.475A>T	ENSP00000356367.1:p.Asn159Tyr
ENST00000367399.6:c.1996A>T	ENSP00000356369.2:p.Asn666Tyr
ENST00000367400.7:c.2332A>T	ENSP00000356370.3:p.Asn778Tyr
ENST00000480086.2:n.233A>T
ENST00000484075.5:c.2332A>T	ENSP00000433932.1:p.Asn778Tyr
ENST00000535699.5:c.2125A>T	ENSP00000438786.1:p.Asn709Tyr
ENST00000538660.5:c.2128+5701A>T	ENSP00000438091.1:n.2128+5701A>T
NM_001193640.1:c.1996A>T	NP_001180569.1:p.Asn666Tyr
NM_001257965.1:c.2125A>T	NP_001244894.1:p.Asn709Tyr
NM_001257966.1:c.2128+5701A>T	NP_001244895.1:n.2128+5701A>T
NM_201253.2:c.2332A>T	NP_957705.1:p.Asn778Tyr
NR_047563.1:n.2333A>T
NR_047564.1:n.2541A>T
XM_011509365.1:c.2332A>T	XP_011507667.1:p.Asn778Tyr
XM_011509366.1:c.2332A>T	XP_011507668.1:p.Asn778Tyr
XM_011509367.1:c.2332A>T	XP_011507669.1:p.Asn778Tyr
XM_011509368.1:c.1750A>T	XP_011507670.1:p.Asn584Tyr
XM_011509369.1:c.775A>T	XP_011507671.1:p.Asn259Tyr
XM_011509365.2:c.2332A>T	XP_011507667.1:p.Asn778Tyr
XM_011509369.2:c.775A>T	XP_011507671.1:p.Asn259Tyr
XM_017000851.1:c.1489A>T	XP_016856340.1:p.Asn497Tyr
XM_017000852.1:c.2332A>T	XP_016856341.1:p.Asn778Tyr
NM_201253.3:c.2332A>T MANE Select	NP_957705.1:p.Asn778Tyr
NM_001193640.2:c.1996A>T	NP_001180569.1:p.Asn666Tyr
NM_001257965.2:c.2125A>T	NP_001244894.1:p.Asn709Tyr
NR_047563.2:n.2285A>T
NR_047564.2:n.2493A>T
NM_001257966.2:c.2128+5701A>T	NP_001244895.1:n.2128+5701A>T