Canonical Allele Identifier: CA7988584

Gene: CD19

Linked Data

• ClinVar Variation Id: 2195580
• ClinVar RCV Id: RCV002628782
• dbSNP Id: rs778238748
• ExAC: 16:28948441 G / C
• gnomAD v2: 16-28948441-G-C
• gnomAD v3: 16-28937120-G-C
• gnomAD v4: 16-28937120-G-C
• MyVariant Identifiers: chr16:g.28948441G>C (hg19) ; chr16:g.28937120G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937120G>C , CM000678.2:g.28937120G>C	GRCh38
NC_000016.9:g.28948441G>C , CM000678.1:g.28948441G>C	GRCh37
NC_000016.8:g.28855942G>C	NCBI36
NG_007275.1:g.10182G>C , LRG_35:g.10182G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1182G>C	ENSP00000313419.4:p.Arg394=
ENST00000538922.8:c.1182G>C MANE Select	ENSP00000437940.2:p.Arg394=
ENST00000324662.7:c.1182G>C	ENSP00000313419.3:p.Arg394=
ENST00000538922.5:c.1182G>C	ENSP00000437940.1:p.Arg394=
ENST00000565089.5:n.1516G>C
ENST00000567368.1:n.322G>C
ENST00000567541.5:c.1182G>C	ENSP00000456201.1:p.Arg394=
ENST00000611258.4:c.1182G>C	ENSP00000481090.1:p.Arg394=
NM_001178098.1:c.1182G>C	NP_001171569.1:p.Arg394=
NM_001770.5:c.1182G>C , LRG_35t1:c.1182G>C	NP_001761.3:p.Arg394=
XM_006721103.2:c.915G>C	XP_006721166.1:p.Arg305=
XM_006721103.3:c.915G>C	XP_006721166.1:p.Arg305=
XM_017023893.1:c.915G>C	XP_016879382.1:p.Arg305=
NM_001178098.2:c.1182G>C	NP_001171569.1:p.Arg394=
NM_001770.6:c.1182G>C MANE Select	NP_001761.3:p.Arg394=
NM_001385732.1:c.915G>C	NP_001372661.1:p.Arg305=
NR_169755.1:n.1524G>C