Canonical Allele Identifier: CA228009

Gene: CRB1

Linked Data

• ClinVar Variation Id: 99880
• ClinVar RCV Id: RCV000086320 ; RCV001250636
• dbSNP Id: rs62636269
• MyVariant Identifiers: chr1:g.197396934G>T (hg19) ; chr1:g.197427804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427804G>T , CM000663.2:g.197427804G>T	GRCh38
NC_000001.10:g.197396934G>T , CM000663.1:g.197396934G>T	GRCh37
NC_000001.9:g.195663557G>T	NCBI36
NG_008483.1:g.164527G>T
NG_008483.2:g.231343G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2479G>T MANE Select	ENSP00000356370.3:p.Gly827Ter
ENST00000638467.1:c.2479G>T	ENSP00000491102.1:p.Gly827Ter
ENST00000681519.1:c.1360G>T	ENSP00000505267.1:p.Gly454Ter
ENST00000367397.1:c.622G>T	ENSP00000356367.1:p.Gly208Ter
ENST00000367399.6:c.2143G>T	ENSP00000356369.2:p.Gly715Ter
ENST00000367400.7:c.2479G>T	ENSP00000356370.3:p.Gly827Ter
ENST00000480086.2:n.380G>T
ENST00000484075.5:c.2479G>T	ENSP00000433932.1:p.Gly827Ter
ENST00000535699.5:c.2272G>T	ENSP00000438786.1:p.Gly758Ter
ENST00000538660.5:c.2128+5848G>T	ENSP00000438091.1:n.2128+5848G>T
NM_001193640.1:c.2143G>T	NP_001180569.1:p.Gly715Ter
NM_001257965.1:c.2272G>T	NP_001244894.1:p.Gly758Ter
NM_001257966.1:c.2128+5848G>T	NP_001244895.1:n.2128+5848G>T
NM_201253.2:c.2479G>T	NP_957705.1:p.Gly827Ter
NR_047563.1:n.2480G>T
NR_047564.1:n.2688G>T
XM_011509365.1:c.2479G>T	XP_011507667.1:p.Gly827Ter
XM_011509366.1:c.2479G>T	XP_011507668.1:p.Gly827Ter
XM_011509367.1:c.2479G>T	XP_011507669.1:p.Gly827Ter
XM_011509368.1:c.1897G>T	XP_011507670.1:p.Gly633Ter
XM_011509369.1:c.922G>T	XP_011507671.1:p.Gly308Ter
XM_011509365.2:c.2479G>T	XP_011507667.1:p.Gly827Ter
XM_011509369.2:c.922G>T	XP_011507671.1:p.Gly308Ter
XM_017000851.1:c.1636G>T	XP_016856340.1:p.Gly546Ter
XM_017000852.1:c.2479G>T	XP_016856341.1:p.Gly827Ter
NM_201253.3:c.2479G>T MANE Select	NP_957705.1:p.Gly827Ter
NM_001193640.2:c.2143G>T	NP_001180569.1:p.Gly715Ter
NM_001257965.2:c.2272G>T	NP_001244894.1:p.Gly758Ter
NR_047563.2:n.2432G>T
NR_047564.2:n.2640G>T
NM_001257966.2:c.2128+5848G>T	NP_001244895.1:n.2128+5848G>T