Canonical Allele Identifier: CA307724196

Gene: CD22

Linked Data

• dbSNP Id: rs1026590934
• gnomAD v3: 19-35333134-G-T
• gnomAD v4: 19-35333134-G-T
• MyVariant Identifiers: chr19:g.35824037G>T (hg19) ; chr19:g.35333134G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35333134G>T , CM000681.2:g.35333134G>T	GRCh38
NC_000019.9:g.35824037G>T , CM000681.1:g.35824037G>T	GRCh37
NC_000019.8:g.40515877G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000085219.10:c.412+210G>T MANE Select	ENSP00000085219.4:n.412+210G>T
ENST00000085219.9:c.412+210G>T	ENSP00000085219.4:n.412+210G>T
ENST00000270311.10:c.412+210G>T	ENSP00000270311.7:n.412+210G>T
ENST00000341773.10:c.412+210G>T	ENSP00000339349.6:n.412+210G>T
ENST00000419549.6:c.9+210G>T	ENSP00000403822.2:n.9+210G>T
ENST00000536635.6:c.412+210G>T	ENSP00000442279.1:n.412+210G>T
ENST00000544992.6:c.412+210G>T	ENSP00000441237.1:n.412+210G>T
ENST00000593867.5:c.412+210G>T	ENSP00000471972.1:n.412+210G>T
ENST00000594250.5:c.412+210G>T	ENSP00000469984.1:n.412+210G>T
ENST00000594349.1:c.379+210G>T	ENSP00000470724.1:n.379+210G>T
ENST00000596492.5:n.950+210G>T
ENST00000597433.1:n.430+210G>T
ENST00000597916.5:c.406+210G>T	ENSP00000472762.1:n.406+210G>T
ENST00000598028.5:n.45-2902G>T
ENST00000598138.5:n.442+210G>T
ENST00000598815.5:n.44+3904G>T
ENST00000599717.5:c.*264+210G>T	ENSP00000470681.1:n.*264+210G>T
ENST00000599811.5:c.412+210G>T	ENSP00000469523.1:n.412+210G>T
ENST00000600131.5:c.406+210G>T	ENSP00000469503.1:n.406+210G>T
ENST00000600424.5:c.406+210G>T	ENSP00000471399.1:n.406+210G>T
ENST00000600655.1:n.36+3904G>T
ENST00000600905.5:n.375+210G>T
ENST00000601329.5:n.43+3904G>T
ENST00000601414.5:n.432+210G>T
ENST00000601732.5:n.316+210G>T
ENST00000601769.5:c.406+210G>T	ENSP00000470193.1:n.406+210G>T
NM_001185099.1:c.412+210G>T	NP_001172028.1:n.412+210G>T
NM_001185100.1:c.412+210G>T	NP_001172029.1:n.412+210G>T
NM_001185101.1:c.412+210G>T	NP_001172030.1:n.412+210G>T
NM_001278417.1:c.9+210G>T	NP_001265346.1:n.9+210G>T
NM_001771.3:c.412+210G>T	NP_001762.2:n.412+210G>T
NM_001771.4:c.412+210G>T MANE Select	NP_001762.2:n.412+210G>T
NM_001185099.2:c.412+210G>T	NP_001172028.1:n.412+210G>T
NM_001185100.2:c.412+210G>T	NP_001172029.1:n.412+210G>T
NM_001278417.2:c.9+210G>T	NP_001265346.1:n.9+210G>T
NM_001185101.2:c.412+210G>T	NP_001172030.1:n.412+210G>T