Canonical Allele Identifier: CA14641593
Gene: CD22 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10419538

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35333116C>G , CM000681.2:g.35333116C>G GRCh38
NC_000019.8:g.40515859C>G NCBI36
NC_000019.9:g.35824019C>G , CM000681.1:g.35824019C>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000085219.9:c.412+192C>G ENSP00000085219.4:p.=
ENST00000270311.10:c.412+192C>G ENSP00000270311.7:p.=
ENST00000341773.10:c.412+192C>G ENSP00000339349.6:p.=
ENST00000419549.6:c.9+192C>G ENSP00000403822.2:p.=
ENST00000536635.6:c.412+192C>G ENSP00000442279.1:p.=
ENST00000544992.6:c.412+192C>G ENSP00000441237.1:p.=
ENST00000593867.5:c.412+192C>G ENSP00000471972.1:p.=
ENST00000594250.5:c.412+192C>G ENSP00000469984.1:p.=
ENST00000594349.1:n.379+192C>G ENSP00000470724.1:p.=
ENST00000596492.5:n.950+192C>G
ENST00000597433.1:n.430+192C>G
ENST00000597916.5:c.406+192C>G ENSP00000472762.1:p.=
ENST00000598028.5:n.45-2920C>G
ENST00000598138.5:n.442+192C>G
ENST00000598815.5:n.44+3886C>G
ENST00000599717.5:c.*264+192C>G ENSP00000470681.1:p.=
ENST00000599811.5:c.412+192C>G ENSP00000469523.1:p.=
ENST00000600131.5:c.406+192C>G ENSP00000469503.1:p.=
ENST00000600424.5:c.406+192C>G ENSP00000471399.1:p.=
ENST00000600655.1:n.36+3886C>G
ENST00000600905.5:n.375+192C>G
ENST00000601329.5:n.43+3886C>G
ENST00000601414.5:n.432+192C>G
ENST00000601732.5:n.316+192C>G
ENST00000601769.5:c.406+192C>G ENSP00000470193.1:p.=
NM_001185099.1:c.412+192C>G VV NP_001172028.1:p.=
NM_001185100.1:c.412+192C>G VV NP_001172029.1:p.=
NM_001185101.1:c.412+192C>G VV NP_001172030.1:p.=
NM_001278417.1:c.9+192C>G VV NP_001265346.1:p.=
NM_001771.3:c.412+192C>G VV NP_001762.2:p.=