Canonical Allele Identifier: CA2632551748

Gene: CD19

Linked Data

• gnomAD v4: 16-28936994-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28936998del , CM000678.2:g.28936998del	GRCh38
NC_000016.9:g.28948319del , CM000678.1:g.28948319del	GRCh37
NC_000016.8:g.28855820del	NCBI36
NG_007275.1:g.10060del , LRG_35:g.10060del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1085-25del	ENSP00000313419.4:n.1085-25del
ENST00000538922.8:c.1085-25del MANE Select	ENSP00000437940.2:n.1085-25del
ENST00000324662.7:c.1085-25del	ENSP00000313419.3:n.1085-25del
ENST00000538922.5:c.1085-25del	ENSP00000437940.1:n.1085-25del
ENST00000565089.5:n.1419-25del
ENST00000567368.1:n.200del
ENST00000567541.5:c.1085-25del	ENSP00000456201.1:n.1085-25del
ENST00000611258.4:c.1085-25del	ENSP00000481090.1:n.1085-25del
NM_001178098.1:c.1085-25del	NP_001171569.1:n.1085-25del
NM_001770.5:c.1085-25del , LRG_35t1:c.1085-25del	NP_001761.3:n.1085-25del
XM_006721103.2:c.818-25del	XP_006721166.1:n.818-25del
XR_950871.1:n.1098-25del
XR_950872.1:n.987-25del
XM_006721103.3:c.818-25del	XP_006721166.1:n.818-25del
XM_017023893.1:c.818-25del	XP_016879382.1:n.818-25del
XR_950871.2:n.1081-25del
NM_001178098.2:c.1085-25del	NP_001171569.1:n.1085-25del
NM_001770.6:c.1085-25del MANE Select	NP_001761.3:n.1085-25del
NM_001385732.1:c.818-25del	NP_001372661.1:n.818-25del
NR_169755.1:n.1427-25del