Canonical Allele Identifier: CA344036941

Gene: CRB1

Linked Data

• ClinVar Variation Id: 849050
• ClinVar RCV Id: RCV001052934
• dbSNP Id: rs62636287
• MyVariant Identifiers: chr1:g.197396761G>C (hg19) ; chr1:g.197427631G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427631G>C , CM000663.2:g.197427631G>C	GRCh38
NC_000001.10:g.197396761G>C , CM000663.1:g.197396761G>C	GRCh37
NC_000001.9:g.195663384G>C	NCBI36
NG_008483.1:g.164354G>C
NG_008483.2:g.231170G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2306G>C MANE Select	ENSP00000356370.3:p.Arg769Pro
ENST00000638467.1:c.2306G>C	ENSP00000491102.1:p.Arg769Pro
ENST00000681519.1:c.1187G>C	ENSP00000505267.1:p.Arg396Pro
ENST00000367397.1:c.449G>C	ENSP00000356367.1:p.Arg150Pro
ENST00000367399.6:c.1970G>C	ENSP00000356369.2:p.Arg657Pro
ENST00000367400.7:c.2306G>C	ENSP00000356370.3:p.Arg769Pro
ENST00000480086.2:n.207G>C
ENST00000484075.5:c.2306G>C	ENSP00000433932.1:p.Arg769Pro
ENST00000535699.5:c.2099G>C	ENSP00000438786.1:p.Arg700Pro
ENST00000538660.5:c.2128+5675G>C	ENSP00000438091.1:n.2128+5675G>C
NM_001193640.1:c.1970G>C	NP_001180569.1:p.Arg657Pro
NM_001257965.1:c.2099G>C	NP_001244894.1:p.Arg700Pro
NM_001257966.1:c.2128+5675G>C	NP_001244895.1:n.2128+5675G>C
NM_201253.2:c.2306G>C	NP_957705.1:p.Arg769Pro
NR_047563.1:n.2307G>C
NR_047564.1:n.2515G>C
XM_011509365.1:c.2306G>C	XP_011507667.1:p.Arg769Pro
XM_011509366.1:c.2306G>C	XP_011507668.1:p.Arg769Pro
XM_011509367.1:c.2306G>C	XP_011507669.1:p.Arg769Pro
XM_011509368.1:c.1724G>C	XP_011507670.1:p.Arg575Pro
XM_011509369.1:c.749G>C	XP_011507671.1:p.Arg250Pro
XM_011509365.2:c.2306G>C	XP_011507667.1:p.Arg769Pro
XM_011509369.2:c.749G>C	XP_011507671.1:p.Arg250Pro
XM_017000851.1:c.1463G>C	XP_016856340.1:p.Arg488Pro
XM_017000852.1:c.2306G>C	XP_016856341.1:p.Arg769Pro
NM_201253.3:c.2306G>C MANE Select	NP_957705.1:p.Arg769Pro
NM_001193640.2:c.1970G>C	NP_001180569.1:p.Arg657Pro
NM_001257965.2:c.2099G>C	NP_001244894.1:p.Arg700Pro
NR_047563.2:n.2259G>C
NR_047564.2:n.2467G>C
NM_001257966.2:c.2128+5675G>C	NP_001244895.1:n.2128+5675G>C