Canonical Allele Identifier: CA719707431

Gene: CD19

Linked Data

• dbSNP Id: rs1405448790
• gnomAD v3: 16-28937795-TG-T
• gnomAD v4: 16-28937795-TG-T
• MyVariant Identifiers: chr16:g.28949117del (hg19) ; chr16:g.28937796del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937798del , CM000678.2:g.28937798del	GRCh38
NC_000016.9:g.28949119del , CM000678.1:g.28949119del	GRCh37
NC_000016.8:g.28856620del	NCBI36
NG_007275.1:g.10860del , LRG_35:g.10860del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1459del	ENSP00000313419.4:p.Asp487ThrfsTer18
ENST00000538922.8:c.1459del MANE Select	ENSP00000437940.2:p.Asp487ThrfsTer17
ENST00000324662.7:c.1459del	ENSP00000313419.3:p.Asp487ThrfsTer17
ENST00000538922.5:c.1459del	ENSP00000437940.1:p.Asp487ThrfsTer18
ENST00000565089.5:n.1893del
ENST00000567368.1:n.569+118del
ENST00000567541.5:c.1459del	ENSP00000456201.1:p.Asp487ThrfsTer18
ENST00000611258.4:c.*54del	ENSP00000481090.1:n.*54del
NM_001178098.1:c.1459del	NP_001171569.1:p.Asp487ThrfsTer18
NM_001770.5:c.1459del , LRG_35t1:c.1459del	NP_001761.3:p.Asp487ThrfsTer17
XM_006721103.2:c.1192del	XP_006721166.1:p.Asp398ThrfsTer18
XM_006721103.3:c.1192del	XP_006721166.1:p.Asp398ThrfsTer18
XM_017023893.1:c.1192del	XP_016879382.1:p.Asp398ThrfsTer17
NM_001178098.2:c.1459del	NP_001171569.1:p.Asp487ThrfsTer18
NM_001770.6:c.1459del MANE Select	NP_001761.3:p.Asp487ThrfsTer17
NM_001385732.1:c.1192del	NP_001372661.1:p.Asp398ThrfsTer17
NR_169755.1:n.1801del