Canonical Allele Identifier: CA279220244

Gene: CD19

Linked Data

• dbSNP Id: rs912760554
• gnomAD v2: 16-28949246-C-CT
• gnomAD v3: 16-28937925-C-CT
• gnomAD v4: 16-28937925-C-CT
• MyVariant Identifiers: chr16:g.28949246_28949247insT (hg19) ; chr16:g.28937925_28937926insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937925_28937926insT , CM000678.2:g.28937925_28937926insT	GRCh38
NC_000016.9:g.28949246_28949247insT , CM000678.1:g.28949246_28949247insT	GRCh37
NC_000016.8:g.28856747_28856748insT	NCBI36
NG_007275.1:g.10987_10988insT , LRG_35:g.10987_10988insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1486+100_1486+101insT	ENSP00000313419.4:n.1486+100_1486+101insT
ENST00000538922.8:c.1486+100_1486+101insT MANE Select	ENSP00000437940.2:n.1486+100_1486+101insT
ENST00000324662.7:c.1486+100_1486+101insT	ENSP00000313419.3:n.1486+100_1486+101insT
ENST00000538922.5:c.1486+100_1486+101insT	ENSP00000437940.1:n.1486+100_1486+101insT
ENST00000565089.5:n.1920+100_1920+101insT
ENST00000567368.1:n.569+245_569+246insT
ENST00000567541.5:c.1486+100_1486+101insT	ENSP00000456201.1:n.1486+100_1486+101insT
ENST00000611258.4:c.*81+100_*81+101insT	ENSP00000481090.1:n.*81+100_*81+101insT
NM_001178098.1:c.1486+100_1486+101insT	NP_001171569.1:n.1486+100_1486+101insT
NM_001770.5:c.1486+100_1486+101insT , LRG_35t1:c.1486+100_1486+101insT	NP_001761.3:n.1486+100_1486+101insT
XM_006721103.2:c.1219+100_1219+101insT	XP_006721166.1:n.1219+100_1219+101insT
XM_006721103.3:c.1219+100_1219+101insT	XP_006721166.1:n.1219+100_1219+101insT
XM_017023893.1:c.1219+100_1219+101insT	XP_016879382.1:n.1219+100_1219+101insT
NM_001178098.2:c.1486+100_1486+101insT	NP_001171569.1:n.1486+100_1486+101insT
NM_001770.6:c.1486+100_1486+101insT MANE Select	NP_001761.3:n.1486+100_1486+101insT
NM_001385732.1:c.1219+100_1219+101insT	NP_001372661.1:n.1219+100_1219+101insT
NR_169755.1:n.1828+100_1828+101insT