Canonical Allele Identifier: CA35895908

Gene: CRB1

Linked Data

• dbSNP Id: rs376992575
• gnomAD v3: 1-197477911-C-A
• gnomAD v4: 1-197477911-C-A
• MyVariant Identifiers: chr1:g.197447041C>A (hg19) ; chr1:g.197477911C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477911C>A , CM000663.2:g.197477911C>A	GRCh38
NC_000001.10:g.197447041C>A , CM000663.1:g.197447041C>A	GRCh37
NC_000001.9:g.195713664C>A	NCBI36
NG_008483.1:g.214634C>A
NG_008483.2:g.281450C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.*32C>A MANE Select	ENSP00000356370.3:n.*32C>A
ENST00000367400.7:c.*32C>A	ENSP00000356370.3:n.*32C>A
ENST00000448952.1:c.487C>A	ENSP00000395407.1:n.487C>A
ENST00000484075.5:c.*364C>A	ENSP00000433932.1:n.*364C>A
ENST00000535699.5:c.*32C>A	ENSP00000438786.1:n.*32C>A
ENST00000538660.5:c.*32C>A	ENSP00000438091.1:n.*32C>A
NM_001193640.1:c.*32C>A	NP_001180569.1:n.*32C>A
NM_001257965.1:c.*32C>A	NP_001244894.1:n.*32C>A
NM_001257966.1:c.*32C>A	NP_001244895.1:n.*32C>A
NM_201253.2:c.*32C>A	NP_957705.1:n.*32C>A
NR_047563.1:n.4254C>A
NR_047564.1:n.4704C>A
XM_011509366.1:c.*358C>A	XP_011507668.1:n.*358C>A
XM_011509367.1:c.*232C>A	XP_011507669.1:n.*232C>A
XM_011509368.1:c.*32C>A	XP_011507670.1:n.*32C>A
XM_011509369.1:c.*32C>A	XP_011507671.1:n.*32C>A
XM_011509369.2:c.*32C>A	XP_011507671.1:n.*32C>A
XM_017000851.1:c.*32C>A	XP_016856340.1:n.*32C>A
XM_017000852.1:c.*32C>A	XP_016856341.1:n.*32C>A
NM_201253.3:c.*32C>A MANE Select	NP_957705.1:n.*32C>A
NM_001193640.2:c.*32C>A	NP_001180569.1:n.*32C>A
NM_001257965.2:c.*32C>A	NP_001244894.1:n.*32C>A
NR_047563.2:n.4206C>A
NR_047564.2:n.4656C>A
NM_001257966.2:c.*32C>A	NP_001244895.1:n.*32C>A