Canonical Allele Identifier: CA422672274

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1921937
• ClinVar RCV Id: RCV002613410
• MyVariant Identifiers: chr1:g.197398617G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429487G>T , CM000663.2:g.197429487G>T	GRCh38
NC_000001.10:g.197398617G>T , CM000663.1:g.197398617G>T	GRCh37
NC_000001.9:g.195665240G>T	NCBI36
NG_008483.1:g.166210G>T
NG_008483.2:g.233026G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2715G>T MANE Select	ENSP00000356370.3:p.Arg905=
ENST00000638467.1:c.2715G>T	ENSP00000491102.1:p.Arg905=
ENST00000681519.1:c.1596G>T	ENSP00000505267.1:p.Arg532=
ENST00000367397.1:c.858G>T	ENSP00000356367.1:p.Arg286=
ENST00000367399.6:c.2379G>T	ENSP00000356369.2:p.Arg793=
ENST00000367400.7:c.2715G>T	ENSP00000356370.3:p.Arg905=
ENST00000484075.5:c.2715G>T	ENSP00000433932.1:p.Arg905=
ENST00000535699.5:c.2643G>T	ENSP00000438786.1:p.Arg881=
ENST00000538660.5:c.2129-6113G>T	ENSP00000438091.1:n.2129-6113G>T
NM_001193640.1:c.2379G>T	NP_001180569.1:p.Arg793=
NM_001257965.1:c.2643G>T	NP_001244894.1:p.Arg881=
NM_001257966.1:c.2129-6113G>T	NP_001244895.1:n.2129-6113G>T
NM_201253.2:c.2715G>T	NP_957705.1:p.Arg905=
NR_047563.1:n.2716G>T
NR_047564.1:n.2924G>T
XM_011509365.1:c.2715G>T	XP_011507667.1:p.Arg905=
XM_011509366.1:c.2715G>T	XP_011507668.1:p.Arg905=
XM_011509367.1:c.2715G>T	XP_011507669.1:p.Arg905=
XM_011509368.1:c.2133G>T	XP_011507670.1:p.Arg711=
XM_011509369.1:c.1158G>T	XP_011507671.1:p.Arg386=
XM_011509365.2:c.2715G>T	XP_011507667.1:p.Arg905=
XM_011509369.2:c.1158G>T	XP_011507671.1:p.Arg386=
XM_017000851.1:c.1872G>T	XP_016856340.1:p.Arg624=
XM_017000852.1:c.2850G>T	XP_016856341.1:p.Arg950=
NM_201253.3:c.2715G>T MANE Select	NP_957705.1:p.Arg905=
NM_001193640.2:c.2379G>T	NP_001180569.1:p.Arg793=
NM_001257965.2:c.2643G>T	NP_001244894.1:p.Arg881=
NR_047563.2:n.2668G>T
NR_047564.2:n.2876G>T
NM_001257966.2:c.2129-6113G>T	NP_001244895.1:n.2129-6113G>T