Canonical Allele Identifier: CA7988693

Gene: CD19

Linked Data

• ClinVar Variation Id: 1529162
• ClinVar RCV Id: RCV002096946
• dbSNP Id: rs373911415
• ExAC: 16:28949074 C / G
• gnomAD v2: 16-28949074-C-G
• gnomAD v3: 16-28937753-C-G
• gnomAD v4: 16-28937753-C-G
• MyVariant Identifiers: chr16:g.28949074C>G (hg19) ; chr16:g.28937753C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937753C>G , CM000678.2:g.28937753C>G	GRCh38
NC_000016.9:g.28949074C>G , CM000678.1:g.28949074C>G	GRCh37
NC_000016.8:g.28856575C>G	NCBI36
NG_007275.1:g.10815C>G , LRG_35:g.10815C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1430-16C>G	ENSP00000313419.4:n.1430-16C>G
ENST00000538922.8:c.1430-16C>G MANE Select	ENSP00000437940.2:n.1430-16C>G
ENST00000324662.7:c.1430-16C>G	ENSP00000313419.3:n.1430-16C>G
ENST00000538922.5:c.1430-16C>G	ENSP00000437940.1:n.1430-16C>G
ENST00000565089.5:n.1864-16C>G
ENST00000567368.1:n.569+73C>G
ENST00000567541.5:c.1430-16C>G	ENSP00000456201.1:n.1430-16C>G
ENST00000611258.4:c.*25-16C>G	ENSP00000481090.1:n.*25-16C>G
NM_001178098.1:c.1430-16C>G	NP_001171569.1:n.1430-16C>G
NM_001770.5:c.1430-16C>G , LRG_35t1:c.1430-16C>G	NP_001761.3:n.1430-16C>G
XM_006721103.2:c.1163-16C>G	XP_006721166.1:n.1163-16C>G
XM_006721103.3:c.1163-16C>G	XP_006721166.1:n.1163-16C>G
XM_017023893.1:c.1163-16C>G	XP_016879382.1:n.1163-16C>G
NM_001178098.2:c.1430-16C>G	NP_001171569.1:n.1430-16C>G
NM_001770.6:c.1430-16C>G MANE Select	NP_001761.3:n.1430-16C>G
NM_001385732.1:c.1163-16C>G	NP_001372661.1:n.1163-16C>G
NR_169755.1:n.1772-16C>G