Canonical Allele Identifier: CA622162936

Gene: CD19

Linked Data

• dbSNP Id: rs1357949552
• gnomAD v2: 16-28948664-ACTCCAACCTTGGGCAGGACCAGCTCTCCCAGGGTAAGGCTGCC-A
• gnomAD v4: 16-28937343-ACTCCAACCTTGGGCAGGACCAGCTCTCCCAGGGTAAGGCTGCC-A
• MyVariant Identifiers: chr16:g.28948665_28948707del (hg19) ; chr16:g.28937344_28937386del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937348_28937390del , CM000678.2:g.28937348_28937390del	GRCh38
NC_000016.9:g.28948669_28948711del , CM000678.1:g.28948669_28948711del	GRCh37
NC_000016.8:g.28856170_28856212del	NCBI36
NG_007275.1:g.10410_10452del , LRG_35:g.10410_10452del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1276_1303+15del
ENST00000538922.8:c.1276_1303+15del
ENST00000324662.7:c.1276_1303+15del
ENST00000538922.5:c.1276_1303+15del
ENST00000565089.5:n.1610_1637+15del
ENST00000567368.1:n.416_443+15del
ENST00000567541.5:c.1276_1303+15del
ENST00000611258.4:c.1275_1302+15del
NM_001178098.1:c.1276_1303+15del
NM_001770.5:c.1276_1303+15del , LRG_35t1:c.1276_1303+15del
XM_006721103.2:c.1009_1036+15del
XM_006721103.3:c.1009_1036+15del
XM_017023893.1:c.1009_1036+15del
NM_001178098.2:c.1276_1303+15del
NM_001770.6:c.1276_1303+15del
NM_001385732.1:c.1009_1036+15del
NR_169755.1:n.1618_1645+15del