Canonical Allele Identifier: CA2333614811
Gene: CD22 HGNC NCBI

Linked Data

dbSNP Id: rs10413500

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35345923C>A , CM000681.2:g.35345923C>A GRCh38
NC_000019.9:g.35836826C>A , CM000681.1:g.35836826C>A GRCh37
NC_000019.8:g.40528666C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000085219.10:c.2327+203C>A MANE Select ENSP00000085219.4:n.2327+203C>A
ENST00000085219.9:c.2327+203C>A ENSP00000085219.4:n.2327+203C>A
ENST00000270311.10:c.1796+203C>A ENSP00000270311.7:n.1796+203C>A
ENST00000341773.10:c.1796+203C>A ENSP00000339349.6:n.1796+203C>A
ENST00000419549.6:c.1811+203C>A ENSP00000403822.2:n.1811+203C>A
ENST00000536635.6:c.2063+203C>A ENSP00000442279.1:n.2063+203C>A
ENST00000544992.6:c.2209-228C>A ENSP00000441237.1:n.2209-228C>A
ENST00000594250.5:c.1796+203C>A ENSP00000469984.1:n.1796+203C>A
ENST00000601769.5:c.*1632+203C>A ENSP00000470193.1:n.*1632+203C>A
NM_001185099.1:c.2063+203C>A NP_001172028.1:n.2063+203C>A
NM_001185100.1:c.2209-228C>A NP_001172029.1:n.2209-228C>A
NM_001185101.1:c.1796+203C>A NP_001172030.1:n.1796+203C>A
NM_001278417.1:c.1811+203C>A NP_001265346.1:n.1811+203C>A
NM_001771.3:c.2327+203C>A NP_001762.2:n.2327+203C>A
NM_001771.4:c.2327+203C>A MANE Select NP_001762.2:n.2327+203C>A
NM_001185099.2:c.2063+203C>A NP_001172028.1:n.2063+203C>A
NM_001185100.2:c.2209-228C>A NP_001172029.1:n.2209-228C>A
NM_001278417.2:c.1811+203C>A NP_001265346.1:n.1811+203C>A
NM_001185101.2:c.1796+203C>A NP_001172030.1:n.1796+203C>A