Canonical Allele Identifier: CA2215894525

Gene: CD19

Linked Data

• dbSNP Id: rs1964789970
• gnomAD v4: 16-28937050-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937056dup , CM000678.2:g.28937056dup	GRCh38
NC_000016.9:g.28948377dup , CM000678.1:g.28948377dup	GRCh37
NC_000016.8:g.28855878dup	NCBI36
NG_007275.1:g.10118dup , LRG_35:g.10118dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1118dup	ENSP00000313419.4:p.Thr374HisfsTer?
ENST00000538922.8:c.1118dup MANE Select	ENSP00000437940.2:p.Thr374HisfsTer?
ENST00000324662.7:c.1118dup	ENSP00000313419.3:p.Thr374HisfsTer?
ENST00000538922.5:c.1118dup	ENSP00000437940.1:p.Thr374HisfsTer?
ENST00000565089.5:n.1452dup
ENST00000567368.1:n.258dup
ENST00000567541.5:c.1118dup	ENSP00000456201.1:p.Thr374HisfsTer?
ENST00000611258.4:c.1118dup	ENSP00000481090.1:p.Thr374HisfsTer?
NM_001178098.1:c.1118dup	NP_001171569.1:p.Thr374HisfsTer?
NM_001770.5:c.1118dup , LRG_35t1:c.1118dup	NP_001761.3:p.Thr374HisfsTer?
XM_006721103.2:c.851dup	XP_006721166.1:p.Thr285HisfsTer?
XR_950871.1:n.1131dup
XR_950872.1:n.1020dup
XM_006721103.3:c.851dup	XP_006721166.1:p.Thr285HisfsTer?
XM_017023893.1:c.851dup	XP_016879382.1:p.Thr285HisfsTer?
XR_950871.2:n.1114dup
NM_001178098.2:c.1118dup	NP_001171569.1:p.Thr374HisfsTer?
NM_001770.6:c.1118dup MANE Select	NP_001761.3:p.Thr374HisfsTer?
NM_001385732.1:c.851dup	NP_001372661.1:p.Thr285HisfsTer?
NR_169755.1:n.1460dup