Canonical Allele Identifier: CA494489834

Gene: CD19

Linked Data

• gnomAD v4: 16-28937667-C-A
• MyVariant Identifiers: chr16:g.28948988C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937667C>A , CM000678.2:g.28937667C>A	GRCh38
NC_000016.9:g.28948988C>A , CM000678.1:g.28948988C>A	GRCh37
NC_000016.8:g.28856489C>A	NCBI36
NG_007275.1:g.10729C>A , LRG_35:g.10729C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1416C>A	ENSP00000313419.4:p.Val472=
ENST00000538922.8:c.1416C>A MANE Select	ENSP00000437940.2:p.Val472=
ENST00000324662.7:c.1416C>A	ENSP00000313419.3:p.Val472=
ENST00000538922.5:c.1416C>A	ENSP00000437940.1:p.Val472=
ENST00000565089.5:n.1850C>A
ENST00000567368.1:n.556C>A
ENST00000567541.5:c.1416C>A	ENSP00000456201.1:p.Val472=
ENST00000611258.4:c.*11C>A	ENSP00000481090.1:n.*11C>A
NM_001178098.1:c.1416C>A	NP_001171569.1:p.Val472=
NM_001770.5:c.1416C>A , LRG_35t1:c.1416C>A	NP_001761.3:p.Val472=
XM_006721103.2:c.1149C>A	XP_006721166.1:p.Val383=
XM_006721103.3:c.1149C>A	XP_006721166.1:p.Val383=
XM_017023893.1:c.1149C>A	XP_016879382.1:p.Val383=
NM_001178098.2:c.1416C>A	NP_001171569.1:p.Val472=
NM_001770.6:c.1416C>A MANE Select	NP_001761.3:p.Val472=
NM_001385732.1:c.1149C>A	NP_001372661.1:p.Val383=
NR_169755.1:n.1758C>A