Canonical Allele Identifier: CA344037070

Gene: CRB1

Linked Data

• ClinVar Variation Id: 2925302
• ClinVar RCV Id: RCV003780956
• MyVariant Identifiers: chr1:g.197396826G>C (hg19) ; chr1:g.197427696G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427696G>C , CM000663.2:g.197427696G>C	GRCh38
NC_000001.10:g.197396826G>C , CM000663.1:g.197396826G>C	GRCh37
NC_000001.9:g.195663449G>C	NCBI36
NG_008483.1:g.164419G>C
NG_008483.2:g.231235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2371G>C MANE Select	ENSP00000356370.3:p.Gly791Arg
ENST00000638467.1:c.2371G>C	ENSP00000491102.1:p.Gly791Arg
ENST00000681519.1:c.1252G>C	ENSP00000505267.1:p.Gly418Arg
ENST00000367397.1:c.514G>C	ENSP00000356367.1:p.Gly172Arg
ENST00000367399.6:c.2035G>C	ENSP00000356369.2:p.Gly679Arg
ENST00000367400.7:c.2371G>C	ENSP00000356370.3:p.Gly791Arg
ENST00000480086.2:n.272G>C
ENST00000484075.5:c.2371G>C	ENSP00000433932.1:p.Gly791Arg
ENST00000535699.5:c.2164G>C	ENSP00000438786.1:p.Gly722Arg
ENST00000538660.5:c.2128+5740G>C	ENSP00000438091.1:n.2128+5740G>C
NM_001193640.1:c.2035G>C	NP_001180569.1:p.Gly679Arg
NM_001257965.1:c.2164G>C	NP_001244894.1:p.Gly722Arg
NM_001257966.1:c.2128+5740G>C	NP_001244895.1:n.2128+5740G>C
NM_201253.2:c.2371G>C	NP_957705.1:p.Gly791Arg
NR_047563.1:n.2372G>C
NR_047564.1:n.2580G>C
XM_011509365.1:c.2371G>C	XP_011507667.1:p.Gly791Arg
XM_011509366.1:c.2371G>C	XP_011507668.1:p.Gly791Arg
XM_011509367.1:c.2371G>C	XP_011507669.1:p.Gly791Arg
XM_011509368.1:c.1789G>C	XP_011507670.1:p.Gly597Arg
XM_011509369.1:c.814G>C	XP_011507671.1:p.Gly272Arg
XM_011509365.2:c.2371G>C	XP_011507667.1:p.Gly791Arg
XM_011509369.2:c.814G>C	XP_011507671.1:p.Gly272Arg
XM_017000851.1:c.1528G>C	XP_016856340.1:p.Gly510Arg
XM_017000852.1:c.2371G>C	XP_016856341.1:p.Gly791Arg
NM_201253.3:c.2371G>C MANE Select	NP_957705.1:p.Gly791Arg
NM_001193640.2:c.2035G>C	NP_001180569.1:p.Gly679Arg
NM_001257965.2:c.2164G>C	NP_001244894.1:p.Gly722Arg
NR_047563.2:n.2324G>C
NR_047564.2:n.2532G>C
NM_001257966.2:c.2128+5740G>C	NP_001244895.1:n.2128+5740G>C