Canonical Allele Identifier: CA7988581

Gene: CD19

Linked Data

• ClinVar Variation Id: 2518097
• ClinVar RCV Id: RCV003279294
• dbSNP Id: rs766009282
• ExAC: 16:28948409 G / A
• gnomAD v2: 16-28948409-G-A
• gnomAD v3: 16-28937088-G-A
• gnomAD v4: 16-28937088-G-A
• MyVariant Identifiers: chr16:g.28948409G>A (hg19) ; chr16:g.28937088G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937088G>A , CM000678.2:g.28937088G>A	GRCh38
NC_000016.9:g.28948409G>A , CM000678.1:g.28948409G>A	GRCh37
NC_000016.8:g.28855910G>A	NCBI36
NG_007275.1:g.10150G>A , LRG_35:g.10150G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1150G>A	ENSP00000313419.4:p.Asp384Asn
ENST00000538922.8:c.1150G>A MANE Select	ENSP00000437940.2:p.Asp384Asn
ENST00000324662.7:c.1150G>A	ENSP00000313419.3:p.Asp384Asn
ENST00000538922.5:c.1150G>A	ENSP00000437940.1:p.Asp384Asn
ENST00000565089.5:n.1484G>A
ENST00000567368.1:n.290G>A
ENST00000567541.5:c.1150G>A	ENSP00000456201.1:p.Asp384Asn
ENST00000611258.4:c.1150G>A	ENSP00000481090.1:p.Asp384Asn
NM_001178098.1:c.1150G>A	NP_001171569.1:p.Asp384Asn
NM_001770.5:c.1150G>A , LRG_35t1:c.1150G>A	NP_001761.3:p.Asp384Asn
XM_006721103.2:c.883G>A	XP_006721166.1:p.Asp295Asn
XR_950871.1:n.1163G>A
XR_950872.1:n.1052G>A
XM_006721103.3:c.883G>A	XP_006721166.1:p.Asp295Asn
XM_017023893.1:c.883G>A	XP_016879382.1:p.Asp295Asn
XR_950871.2:n.1146G>A
NM_001178098.2:c.1150G>A	NP_001171569.1:p.Asp384Asn
NM_001770.6:c.1150G>A MANE Select	NP_001761.3:p.Asp384Asn
NM_001385732.1:c.883G>A	NP_001372661.1:p.Asp295Asn
NR_169755.1:n.1492G>A