Canonical Allele Identifier: CA422808837

Gene: CRB1

Linked Data

• ClinVar Variation Id: 799076
• ClinVar RCV Id: RCV000982652
• dbSNP Id: rs1571556490
• MyVariant Identifiers: chr1:g.197404113C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434983C>T , CM000663.2:g.197434983C>T	GRCh38
NC_000001.10:g.197404113C>T , CM000663.1:g.197404113C>T	GRCh37
NC_000001.9:g.195670736C>T	NCBI36
NG_008483.1:g.171706C>T
NG_008483.2:g.238522C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3120C>T MANE Select	ENSP00000356370.3:p.Ser1040=
ENST00000638467.1:c.3120C>T	ENSP00000491102.1:p.Ser1040=
ENST00000681519.1:c.2001C>T	ENSP00000505267.1:p.Ser667=
ENST00000367397.1:c.1263C>T	ENSP00000356367.1:p.Ser421=
ENST00000367399.6:c.2784C>T	ENSP00000356369.2:p.Ser928=
ENST00000367400.7:c.3120C>T	ENSP00000356370.3:p.Ser1040=
ENST00000484075.5:c.3120C>T	ENSP00000433932.1:p.Ser1040=
ENST00000535699.5:c.3048C>T	ENSP00000438786.1:p.Ser1016=
ENST00000538660.5:c.2129-617C>T	ENSP00000438091.1:n.2129-617C>T
NM_001193640.1:c.2784C>T	NP_001180569.1:p.Ser928=
NM_001257965.1:c.3048C>T	NP_001244894.1:p.Ser1016=
NM_001257966.1:c.2129-617C>T	NP_001244895.1:n.2129-617C>T
NM_201253.2:c.3120C>T	NP_957705.1:p.Ser1040=
NR_047563.1:n.3121C>T
NR_047564.1:n.3329C>T
XM_011509365.1:c.3120C>T	XP_011507667.1:p.Ser1040=
XM_011509366.1:c.3120C>T	XP_011507668.1:p.Ser1040=
XM_011509367.1:c.3120C>T	XP_011507669.1:p.Ser1040=
XM_011509368.1:c.2538C>T	XP_011507670.1:p.Ser846=
XM_011509369.1:c.1563C>T	XP_011507671.1:p.Ser521=
XM_011509365.2:c.3120C>T	XP_011507667.1:p.Ser1040=
XM_011509369.2:c.1563C>T	XP_011507671.1:p.Ser521=
XM_017000851.1:c.2277C>T	XP_016856340.1:p.Ser759=
XM_017000852.1:c.3255C>T	XP_016856341.1:p.Ser1085=
NM_201253.3:c.3120C>T MANE Select	NP_957705.1:p.Ser1040=
NM_001193640.2:c.2784C>T	NP_001180569.1:p.Ser928=
NM_001257965.2:c.3048C>T	NP_001244894.1:p.Ser1016=
NR_047563.2:n.3073C>T
NR_047564.2:n.3281C>T
NM_001257966.2:c.2129-617C>T	NP_001244895.1:n.2129-617C>T