Canonical Allele Identifier: CA729758678

Gene: CRB1

Linked Data

• dbSNP Id: rs1245068161
• MyVariant Identifiers: chr1:g.197398508T>A (hg19) ; chr1:g.197429378T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429378T>A , CM000663.2:g.197429378T>A	GRCh38
NC_000001.10:g.197398508T>A , CM000663.1:g.197398508T>A	GRCh37
NC_000001.9:g.195665131T>A	NCBI36
NG_008483.1:g.166101T>A
NG_008483.2:g.232917T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2677-71T>A MANE Select	ENSP00000356370.3:n.2677-71T>A
ENST00000638467.1:c.2677-71T>A	ENSP00000491102.1:n.2677-71T>A
ENST00000681519.1:c.1558-71T>A	ENSP00000505267.1:n.1558-71T>A
ENST00000367397.1:c.820-71T>A	ENSP00000356367.1:n.820-71T>A
ENST00000367399.6:c.2341-71T>A	ENSP00000356369.2:n.2341-71T>A
ENST00000367400.7:c.2677-71T>A	ENSP00000356370.3:n.2677-71T>A
ENST00000484075.5:c.2677-71T>A	ENSP00000433932.1:n.2677-71T>A
ENST00000535699.5:c.2605-71T>A	ENSP00000438786.1:n.2605-71T>A
ENST00000538660.5:c.2129-6222T>A	ENSP00000438091.1:n.2129-6222T>A
NM_001193640.1:c.2341-71T>A	NP_001180569.1:n.2341-71T>A
NM_001257965.1:c.2605-71T>A	NP_001244894.1:n.2605-71T>A
NM_001257966.1:c.2129-6222T>A	NP_001244895.1:n.2129-6222T>A
NM_201253.2:c.2677-71T>A	NP_957705.1:n.2677-71T>A
NR_047563.1:n.2678-71T>A
NR_047564.1:n.2886-71T>A
XM_011509365.1:c.2677-71T>A	XP_011507667.1:n.2677-71T>A
XM_011509366.1:c.2677-71T>A	XP_011507668.1:n.2677-71T>A
XM_011509367.1:c.2677-71T>A	XP_011507669.1:n.2677-71T>A
XM_011509368.1:c.2095-71T>A	XP_011507670.1:n.2095-71T>A
XM_011509369.1:c.1120-71T>A	XP_011507671.1:n.1120-71T>A
XM_011509365.2:c.2677-71T>A	XP_011507667.1:n.2677-71T>A
XM_011509369.2:c.1120-71T>A	XP_011507671.1:n.1120-71T>A
XM_017000851.1:c.1834-71T>A	XP_016856340.1:n.1834-71T>A
XM_017000852.1:c.2812-71T>A	XP_016856341.1:n.2812-71T>A
NM_201253.3:c.2677-71T>A MANE Select	NP_957705.1:n.2677-71T>A
NM_001193640.2:c.2341-71T>A	NP_001180569.1:n.2341-71T>A
NM_001257965.2:c.2605-71T>A	NP_001244894.1:n.2605-71T>A
NR_047563.2:n.2630-71T>A
NR_047564.2:n.2838-71T>A
NM_001257966.2:c.2129-6222T>A	NP_001244895.1:n.2129-6222T>A