Canonical Allele Identifier: CA622162934

Gene: CD19

Linked Data

• dbSNP Id: rs1199217504
• gnomAD v2: 16-28948635-TGAG-T
• gnomAD v4: 16-28937314-TGAG-T
• MyVariant Identifiers: chr16:g.28948636_28948638del (hg19) ; chr16:g.28937315_28937317del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937320_28937322del , CM000678.2:g.28937320_28937322del	GRCh38
NC_000016.9:g.28948641_28948643del , CM000678.1:g.28948641_28948643del	GRCh37
NC_000016.8:g.28856142_28856144del	NCBI36
NG_007275.1:g.10382_10384del , LRG_35:g.10382_10384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1248_1250del	ENSP00000313419.4:p.Glu416del
ENST00000538922.8:c.1248_1250del MANE Select	ENSP00000437940.2:p.Glu416del
ENST00000324662.7:c.1248_1250del	ENSP00000313419.3:p.Glu416del
ENST00000538922.5:c.1248_1250del	ENSP00000437940.1:p.Glu416del
ENST00000565089.5:n.1582_1584del
ENST00000567368.1:n.388_390del
ENST00000567541.5:c.1248_1250del	ENSP00000456201.1:p.Glu416del
ENST00000611258.4:c.1247_1249del	ENSP00000481090.1:p.Arg416del
NM_001178098.1:c.1248_1250del	NP_001171569.1:p.Glu416del
NM_001770.5:c.1248_1250del , LRG_35t1:c.1248_1250del	NP_001761.3:p.Glu416del
XM_006721103.2:c.981_983del	XP_006721166.1:p.Glu327del
XM_006721103.3:c.981_983del	XP_006721166.1:p.Glu327del
XM_017023893.1:c.981_983del	XP_016879382.1:p.Glu327del
NM_001178098.2:c.1248_1250del	NP_001171569.1:p.Glu416del
NM_001770.6:c.1248_1250del MANE Select	NP_001761.3:p.Glu416del
NM_001385732.1:c.981_983del	NP_001372661.1:p.Glu327del
NR_169755.1:n.1590_1592del