Canonical Allele Identifier: CA422808398

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1533190
• ClinVar RCV Id: RCV002087514
• dbSNP Id: rs1178650450
• gnomAD v2: 1-197390707-C-T
• gnomAD v3: 1-197421577-C-T
• gnomAD v4: 1-197421577-C-T
• COSMIC: COSM274658
• MyVariant Identifiers: chr1:g.197390707C>T (hg19) ; chr1:g.197421577C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421577C>T , CM000663.2:g.197421577C>T	GRCh38
NC_000001.10:g.197390707C>T , CM000663.1:g.197390707C>T	GRCh37
NC_000001.9:g.195657330C>T	NCBI36
NG_008483.1:g.158300C>T
NG_008483.2:g.225116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1749C>T MANE Select	ENSP00000356370.3:p.Ile583=
ENST00000638467.1:c.1749C>T	ENSP00000491102.1:p.Ile583=
ENST00000681519.1:c.630C>T	ENSP00000505267.1:p.Ile210=
ENST00000367397.1:c.-109C>T	ENSP00000356367.1:n.-109C>T
ENST00000367399.6:c.1413C>T	ENSP00000356369.2:p.Ile471=
ENST00000367400.7:c.1749C>T	ENSP00000356370.3:p.Ile583=
ENST00000484075.5:c.1749C>T	ENSP00000433932.1:p.Ile583=
ENST00000535699.5:c.1542C>T	ENSP00000438786.1:p.Ile514=
ENST00000538660.5:c.1749C>T	ENSP00000438091.1:p.Ile583=
NM_001193640.1:c.1413C>T	NP_001180569.1:p.Ile471=
NM_001257965.1:c.1542C>T	NP_001244894.1:p.Ile514=
NM_001257966.1:c.1749C>T	NP_001244895.1:p.Ile583=
NM_201253.2:c.1749C>T	NP_957705.1:p.Ile583=
NR_047563.1:n.1922+36C>T
NR_047564.1:n.1958C>T
XM_011509365.1:c.1749C>T	XP_011507667.1:p.Ile583=
XM_011509366.1:c.1749C>T	XP_011507668.1:p.Ile583=
XM_011509367.1:c.1749C>T	XP_011507669.1:p.Ile583=
XM_011509368.1:c.1167C>T	XP_011507670.1:p.Ile389=
XM_011509369.1:c.192C>T	XP_011507671.1:p.Ile64=
XM_011509365.2:c.1749C>T	XP_011507667.1:p.Ile583=
XM_011509369.2:c.192C>T	XP_011507671.1:p.Ile64=
XM_017000851.1:c.906C>T	XP_016856340.1:p.Ile302=
XM_017000852.1:c.1749C>T	XP_016856341.1:p.Ile583=
NM_201253.3:c.1749C>T MANE Select	NP_957705.1:p.Ile583=
NM_001193640.2:c.1413C>T	NP_001180569.1:p.Ile471=
NM_001257965.2:c.1542C>T	NP_001244894.1:p.Ile514=
NR_047563.2:n.1874+36C>T
NR_047564.2:n.1910C>T
NM_001257966.2:c.1749C>T	NP_001244895.1:p.Ile583=