Canonical Allele Identifier: CA2215894894

Gene: CD19

Linked Data

• dbSNP Id: rs1964812163

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937788del , CM000678.2:g.28937788del	GRCh38
NC_000016.9:g.28949109del , CM000678.1:g.28949109del	GRCh37
NC_000016.8:g.28856610del	NCBI36
NG_007275.1:g.10850del , LRG_35:g.10850del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1449del	ENSP00000313419.4:p.Ser484GlnfsTer21
ENST00000538922.8:c.1449del MANE Select	ENSP00000437940.2:p.Ser484GlnfsTer20
ENST00000324662.7:c.1449del	ENSP00000313419.3:p.Ser484GlnfsTer20
ENST00000538922.5:c.1449del	ENSP00000437940.1:p.Ser484GlnfsTer21
ENST00000565089.5:n.1883del
ENST00000567368.1:n.569+108del
ENST00000567541.5:c.1449del	ENSP00000456201.1:p.Ser484GlnfsTer21
ENST00000611258.4:c.*44del	ENSP00000481090.1:n.*44del
NM_001178098.1:c.1449del	NP_001171569.1:p.Ser484GlnfsTer21
NM_001770.5:c.1449del , LRG_35t1:c.1449del	NP_001761.3:p.Ser484GlnfsTer20
XM_006721103.2:c.1182del	XP_006721166.1:p.Ser395GlnfsTer21
XM_006721103.3:c.1182del	XP_006721166.1:p.Ser395GlnfsTer21
XM_017023893.1:c.1182del	XP_016879382.1:p.Ser395GlnfsTer20
NM_001178098.2:c.1449del	NP_001171569.1:p.Ser484GlnfsTer21
NM_001770.6:c.1449del MANE Select	NP_001761.3:p.Ser484GlnfsTer20
NM_001385732.1:c.1182del	NP_001372661.1:p.Ser395GlnfsTer20
NR_169755.1:n.1791del