Canonical Allele Identifier: CA279220194

Gene: CD19

Linked Data

• dbSNP Id: rs900029937
• gnomAD v3: 16-28937250-TC-T
• gnomAD v4: 16-28937250-TC-T
• MyVariant Identifiers: chr16:g.28948572del (hg19) ; chr16:g.28937251del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937254del , CM000678.2:g.28937254del	GRCh38
NC_000016.9:g.28948575del , CM000678.1:g.28948575del	GRCh37
NC_000016.8:g.28856076del	NCBI36
NG_007275.1:g.10316del , LRG_35:g.10316del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1199-17del	ENSP00000313419.4:n.1199-17del
ENST00000538922.8:c.1199-17del MANE Select	ENSP00000437940.2:n.1199-17del
ENST00000324662.7:c.1199-17del	ENSP00000313419.3:n.1199-17del
ENST00000538922.5:c.1199-17del	ENSP00000437940.1:n.1199-17del
ENST00000565089.5:n.1533-17del
ENST00000567368.1:n.339-17del
ENST00000567541.5:c.1199-17del	ENSP00000456201.1:n.1199-17del
ENST00000611258.4:c.1198-17del	ENSP00000481090.1:n.1198-17del
NM_001178098.1:c.1199-17del	NP_001171569.1:n.1199-17del
NM_001770.5:c.1199-17del , LRG_35t1:c.1199-17del	NP_001761.3:n.1199-17del
XM_006721103.2:c.932-17del	XP_006721166.1:n.932-17del
XM_006721103.3:c.932-17del	XP_006721166.1:n.932-17del
XM_017023893.1:c.932-17del	XP_016879382.1:n.932-17del
NM_001178098.2:c.1199-17del	NP_001171569.1:n.1199-17del
NM_001770.6:c.1199-17del MANE Select	NP_001761.3:n.1199-17del
NM_001385732.1:c.932-17del	NP_001372661.1:n.932-17del
NR_169755.1:n.1541-17del