Canonical Allele Identifier: CA7988696

Gene: CD19

Linked Data

• ClinVar Variation Id: 1955916
• ClinVar RCV Id: RCV002695750
• dbSNP Id: rs779280213
• ExAC: 16:28949119 G / T
• gnomAD v2: 16-28949119-G-T
• gnomAD v4: 16-28937798-G-T
• MyVariant Identifiers: chr16:g.28949119G>T (hg19) ; chr16:g.28937798G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937798G>T , CM000678.2:g.28937798G>T	GRCh38
NC_000016.9:g.28949119G>T , CM000678.1:g.28949119G>T	GRCh37
NC_000016.8:g.28856620G>T	NCBI36
NG_007275.1:g.10860G>T , LRG_35:g.10860G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1459G>T	ENSP00000313419.4:p.Asp487Tyr
ENST00000538922.8:c.1459G>T MANE Select	ENSP00000437940.2:p.Asp487Tyr
ENST00000324662.7:c.1459G>T	ENSP00000313419.3:p.Asp487Tyr
ENST00000538922.5:c.1459G>T	ENSP00000437940.1:p.Asp487Tyr
ENST00000565089.5:n.1893G>T
ENST00000567368.1:n.569+118G>T
ENST00000567541.5:c.1459G>T	ENSP00000456201.1:p.Asp487Tyr
ENST00000611258.4:c.*54G>T	ENSP00000481090.1:n.*54G>T
NM_001178098.1:c.1459G>T	NP_001171569.1:p.Asp487Tyr
NM_001770.5:c.1459G>T , LRG_35t1:c.1459G>T	NP_001761.3:p.Asp487Tyr
XM_006721103.2:c.1192G>T	XP_006721166.1:p.Asp398Tyr
XM_006721103.3:c.1192G>T	XP_006721166.1:p.Asp398Tyr
XM_017023893.1:c.1192G>T	XP_016879382.1:p.Asp398Tyr
NM_001178098.2:c.1459G>T	NP_001171569.1:p.Asp487Tyr
NM_001770.6:c.1459G>T MANE Select	NP_001761.3:p.Asp487Tyr
NM_001385732.1:c.1192G>T	NP_001372661.1:p.Asp398Tyr
NR_169755.1:n.1801G>T