Canonical Allele Identifier: CA719706700

Gene: CD19

Linked Data

• dbSNP Id: rs1329620224
• MyVariant Identifiers: chr16:g.28948584_28948585insC (hg19) ; chr16:g.28937263_28937264insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937268dup , CM000678.2:g.28937268dup	GRCh38
NC_000016.9:g.28948589dup , CM000678.1:g.28948589dup	GRCh37
NC_000016.8:g.28856090dup	NCBI36
NG_007275.1:g.10330dup , LRG_35:g.10330dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1199-3dup	ENSP00000313419.4:n.1199-3dup
ENST00000538922.8:c.1199-3dup MANE Select	ENSP00000437940.2:n.1199-3dup
ENST00000324662.7:c.1199-3dup	ENSP00000313419.3:n.1199-3dup
ENST00000538922.5:c.1199-3dup	ENSP00000437940.1:n.1199-3dup
ENST00000565089.5:n.1533-3dup
ENST00000567368.1:n.339-3dup
ENST00000567541.5:c.1199-3dup	ENSP00000456201.1:n.1199-3dup
ENST00000611258.4:c.1198-3dup	ENSP00000481090.1:n.1198-3dup
NM_001178098.1:c.1199-3dup	NP_001171569.1:n.1199-3dup
NM_001770.5:c.1199-3dup , LRG_35t1:c.1199-3dup	NP_001761.3:n.1199-3dup
XM_006721103.2:c.932-3dup	XP_006721166.1:n.932-3dup
XM_006721103.3:c.932-3dup	XP_006721166.1:n.932-3dup
XM_017023893.1:c.932-3dup	XP_016879382.1:n.932-3dup
NM_001178098.2:c.1199-3dup	NP_001171569.1:n.1199-3dup
NM_001770.6:c.1199-3dup MANE Select	NP_001761.3:n.1199-3dup
NM_001385732.1:c.932-3dup	NP_001372661.1:n.932-3dup
NR_169755.1:n.1541-3dup