Canonical Allele Identifier: CA622162988

Gene: CD19

Linked Data

• dbSNP Id: rs1567507794
• gnomAD v2: 16-28949027-A-AG
• gnomAD v3: 16-28937706-A-AG
• gnomAD v4: 16-28937706-A-AG
• MyVariant Identifiers: chr16:g.28949027_28949028insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937712dup , CM000678.2:g.28937712dup	GRCh38
NC_000016.9:g.28949033dup , CM000678.1:g.28949033dup	GRCh37
NC_000016.8:g.28856534dup	NCBI36
NG_007275.1:g.10774dup , LRG_35:g.10774dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1429+32dup	ENSP00000313419.4:n.1429+32dup
ENST00000538922.8:c.1429+32dup MANE Select	ENSP00000437940.2:n.1429+32dup
ENST00000324662.7:c.1429+32dup	ENSP00000313419.3:n.1429+32dup
ENST00000538922.5:c.1429+32dup	ENSP00000437940.1:n.1429+32dup
ENST00000565089.5:n.1863+32dup
ENST00000567368.1:n.569+32dup
ENST00000567541.5:c.1429+32dup	ENSP00000456201.1:n.1429+32dup
ENST00000611258.4:c.*24+32dup	ENSP00000481090.1:n.*24+32dup
NM_001178098.1:c.1429+32dup	NP_001171569.1:n.1429+32dup
NM_001770.5:c.1429+32dup , LRG_35t1:c.1429+32dup	NP_001761.3:n.1429+32dup
XM_006721103.2:c.1162+32dup	XP_006721166.1:n.1162+32dup
XM_006721103.3:c.1162+32dup	XP_006721166.1:n.1162+32dup
XM_017023893.1:c.1162+32dup	XP_016879382.1:n.1162+32dup
NM_001178098.2:c.1429+32dup	NP_001171569.1:n.1429+32dup
NM_001770.6:c.1429+32dup MANE Select	NP_001761.3:n.1429+32dup
NM_001385732.1:c.1162+32dup	NP_001372661.1:n.1162+32dup
NR_169755.1:n.1771+32dup