Canonical Allele Identifier: CA2698122075

Gene: CRB1

Linked Data

• dbSNP Id: rs2125574432

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477918T>G , CM000663.2:g.197477918T>G	GRCh38
NC_000001.10:g.197447048T>G , CM000663.1:g.197447048T>G	GRCh37
NC_000001.9:g.195713671T>G	NCBI36
NG_008483.1:g.214641T>G
NG_008483.2:g.281457T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.*39T>G MANE Select	ENSP00000356370.3:n.*39T>G
ENST00000367400.7:c.*39T>G	ENSP00000356370.3:n.*39T>G
ENST00000448952.1:c.494T>G	ENSP00000395407.1:n.494T>G
ENST00000484075.5:c.*371T>G	ENSP00000433932.1:n.*371T>G
ENST00000535699.5:c.*39T>G	ENSP00000438786.1:n.*39T>G
ENST00000538660.5:c.*39T>G	ENSP00000438091.1:n.*39T>G
NM_001193640.1:c.*39T>G	NP_001180569.1:n.*39T>G
NM_001257965.1:c.*39T>G	NP_001244894.1:n.*39T>G
NM_001257966.1:c.*39T>G	NP_001244895.1:n.*39T>G
NM_201253.2:c.*39T>G	NP_957705.1:n.*39T>G
NR_047563.1:n.4261T>G
NR_047564.1:n.4711T>G
XM_011509366.1:c.*365T>G	XP_011507668.1:n.*365T>G
XM_011509367.1:c.*239T>G	XP_011507669.1:n.*239T>G
XM_011509368.1:c.*39T>G	XP_011507670.1:n.*39T>G
XM_011509369.1:c.*39T>G	XP_011507671.1:n.*39T>G
XM_011509369.2:c.*39T>G	XP_011507671.1:n.*39T>G
XM_017000851.1:c.*39T>G	XP_016856340.1:n.*39T>G
XM_017000852.1:c.*39T>G	XP_016856341.1:n.*39T>G
NM_201253.3:c.*39T>G MANE Select	NP_957705.1:n.*39T>G
NM_001193640.2:c.*39T>G	NP_001180569.1:n.*39T>G
NM_001257965.2:c.*39T>G	NP_001244894.1:n.*39T>G
NR_047563.2:n.4213T>G
NR_047564.2:n.4663T>G
NM_001257966.2:c.*39T>G	NP_001244895.1:n.*39T>G