Canonical Allele Identifier: CA2649672994

Gene: CRB1

Linked Data

• gnomAD v4: 1-197477948-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477948T>G , CM000663.2:g.197477948T>G	GRCh38
NC_000001.10:g.197447078T>G , CM000663.1:g.197447078T>G	GRCh37
NC_000001.9:g.195713701T>G	NCBI36
NG_008483.1:g.214671T>G
NG_008483.2:g.281487T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.*69T>G MANE Select	ENSP00000356370.3:n.*69T>G
ENST00000367400.7:c.*69T>G	ENSP00000356370.3:n.*69T>G
ENST00000448952.1:c.524T>G	ENSP00000395407.1:n.524T>G
ENST00000484075.5:c.*401T>G	ENSP00000433932.1:n.*401T>G
ENST00000535699.5:c.*69T>G	ENSP00000438786.1:n.*69T>G
ENST00000538660.5:c.*69T>G	ENSP00000438091.1:n.*69T>G
NM_001193640.1:c.*69T>G	NP_001180569.1:n.*69T>G
NM_001257965.1:c.*69T>G	NP_001244894.1:n.*69T>G
NM_001257966.1:c.*69T>G	NP_001244895.1:n.*69T>G
NM_201253.2:c.*69T>G	NP_957705.1:n.*69T>G
NR_047563.1:n.4291T>G
NR_047564.1:n.4741T>G
XM_011509366.1:c.*395T>G	XP_011507668.1:n.*395T>G
XM_011509367.1:c.*269T>G	XP_011507669.1:n.*269T>G
XM_011509368.1:c.*69T>G	XP_011507670.1:n.*69T>G
XM_011509369.1:c.*69T>G	XP_011507671.1:n.*69T>G
XM_011509369.2:c.*69T>G	XP_011507671.1:n.*69T>G
XM_017000851.1:c.*69T>G	XP_016856340.1:n.*69T>G
XM_017000852.1:c.*69T>G	XP_016856341.1:n.*69T>G
NM_201253.3:c.*69T>G MANE Select	NP_957705.1:n.*69T>G
NM_001193640.2:c.*69T>G	NP_001180569.1:n.*69T>G
NM_001257965.2:c.*69T>G	NP_001244894.1:n.*69T>G
NR_047563.2:n.4243T>G
NR_047564.2:n.4693T>G
NM_001257966.2:c.*69T>G	NP_001244895.1:n.*69T>G