Canonical Allele Identifier: CA395406192

Gene: CD19

Linked Data

• ClinVar Variation Id: 2537218
• ClinVar RCV Id: RCV003271497
• dbSNP Id: rs901961639
• gnomAD v2: 16-28948660-A-T
• gnomAD v4: 16-28937339-A-T
• MyVariant Identifiers: chr16:g.28948660A>T (hg19) ; chr16:g.28937339A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937339A>T , CM000678.2:g.28937339A>T	GRCh38
NC_000016.9:g.28948660A>T , CM000678.1:g.28948660A>T	GRCh37
NC_000016.8:g.28856161A>T	NCBI36
NG_007275.1:g.10401A>T , LRG_35:g.10401A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1267A>T	ENSP00000313419.4:p.Asn423Tyr
ENST00000538922.8:c.1267A>T MANE Select	ENSP00000437940.2:p.Asn423Tyr
ENST00000324662.7:c.1267A>T	ENSP00000313419.3:p.Asn423Tyr
ENST00000538922.5:c.1267A>T	ENSP00000437940.1:p.Asn423Tyr
ENST00000565089.5:n.1601A>T
ENST00000567368.1:n.407A>T
ENST00000567541.5:c.1267A>T	ENSP00000456201.1:p.Asn423Tyr
ENST00000611258.4:c.1266A>T	ENSP00000481090.1:p.Arg422Ser
NM_001178098.1:c.1267A>T	NP_001171569.1:p.Asn423Tyr
NM_001770.5:c.1267A>T , LRG_35t1:c.1267A>T	NP_001761.3:p.Asn423Tyr
XM_006721103.2:c.1000A>T	XP_006721166.1:p.Asn334Tyr
XM_006721103.3:c.1000A>T	XP_006721166.1:p.Asn334Tyr
XM_017023893.1:c.1000A>T	XP_016879382.1:p.Asn334Tyr
NM_001178098.2:c.1267A>T	NP_001171569.1:p.Asn423Tyr
NM_001770.6:c.1267A>T MANE Select	NP_001761.3:p.Asn423Tyr
NM_001385732.1:c.1000A>T	NP_001372661.1:p.Asn334Tyr
NR_169755.1:n.1609A>T