Canonical Allele Identifier: CA1312248

Gene: CRB1

Linked Data

• dbSNP Id: rs575358595
• ExAC: 1:197403914 C / T
• gnomAD v2: 1-197403914-C-T
• gnomAD v3: 1-197434784-C-T
• gnomAD v4: 1-197434784-C-T
• MyVariant Identifiers: chr1:g.197403914C>T (hg19) ; chr1:g.197434784C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434784C>T , CM000663.2:g.197434784C>T	GRCh38
NC_000001.10:g.197403914C>T , CM000663.1:g.197403914C>T	GRCh37
NC_000001.9:g.195670537C>T	NCBI36
NG_008483.1:g.171507C>T
NG_008483.2:g.238323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2921C>T MANE Select	ENSP00000356370.3:p.Thr974Ile
ENST00000638467.1:c.2921C>T	ENSP00000491102.1:p.Thr974Ile
ENST00000681519.1:c.1802C>T	ENSP00000505267.1:p.Thr601Ile
ENST00000367397.1:c.1064C>T	ENSP00000356367.1:p.Thr355Ile
ENST00000367399.6:c.2585C>T	ENSP00000356369.2:p.Thr862Ile
ENST00000367400.7:c.2921C>T	ENSP00000356370.3:p.Thr974Ile
ENST00000484075.5:c.2921C>T	ENSP00000433932.1:p.Thr974Ile
ENST00000535699.5:c.2849C>T	ENSP00000438786.1:p.Thr950Ile
ENST00000538660.5:c.2129-816C>T	ENSP00000438091.1:n.2129-816C>T
NM_001193640.1:c.2585C>T	NP_001180569.1:p.Thr862Ile
NM_001257965.1:c.2849C>T	NP_001244894.1:p.Thr950Ile
NM_001257966.1:c.2129-816C>T	NP_001244895.1:n.2129-816C>T
NM_201253.2:c.2921C>T	NP_957705.1:p.Thr974Ile
NR_047563.1:n.2922C>T
NR_047564.1:n.3130C>T
XM_011509365.1:c.2921C>T	XP_011507667.1:p.Thr974Ile
XM_011509366.1:c.2921C>T	XP_011507668.1:p.Thr974Ile
XM_011509367.1:c.2921C>T	XP_011507669.1:p.Thr974Ile
XM_011509368.1:c.2339C>T	XP_011507670.1:p.Thr780Ile
XM_011509369.1:c.1364C>T	XP_011507671.1:p.Thr455Ile
XM_011509365.2:c.2921C>T	XP_011507667.1:p.Thr974Ile
XM_011509369.2:c.1364C>T	XP_011507671.1:p.Thr455Ile
XM_017000851.1:c.2078C>T	XP_016856340.1:p.Thr693Ile
XM_017000852.1:c.3056C>T	XP_016856341.1:p.Thr1019Ile
NM_201253.3:c.2921C>T MANE Select	NP_957705.1:p.Thr974Ile
NM_001193640.2:c.2585C>T	NP_001180569.1:p.Thr862Ile
NM_001257965.2:c.2849C>T	NP_001244894.1:p.Thr950Ile
NR_047563.2:n.2874C>T
NR_047564.2:n.3082C>T
NM_001257966.2:c.2129-816C>T	NP_001244895.1:n.2129-816C>T