Canonical Allele Identifier: CA395405583

Gene: CD19

Linked Data

• ClinVar Variation Id: 1471574
• ClinVar RCV Id: RCV001966847
• dbSNP Id: rs1488844762
• gnomAD v2: 16-28948376-G-C
• gnomAD v4: 16-28937055-G-C
• MyVariant Identifiers: chr16:g.28948376G>C (hg19) ; chr16:g.28937055G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937055G>C , CM000678.2:g.28937055G>C	GRCh38
NC_000016.9:g.28948376G>C , CM000678.1:g.28948376G>C	GRCh37
NC_000016.8:g.28855877G>C	NCBI36
NG_007275.1:g.10117G>C , LRG_35:g.10117G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1117G>C	ENSP00000313419.4:p.Gly373Arg
ENST00000538922.8:c.1117G>C MANE Select	ENSP00000437940.2:p.Gly373Arg
ENST00000324662.7:c.1117G>C	ENSP00000313419.3:p.Gly373Arg
ENST00000538922.5:c.1117G>C	ENSP00000437940.1:p.Gly373Arg
ENST00000565089.5:n.1451G>C
ENST00000567368.1:n.257G>C
ENST00000567541.5:c.1117G>C	ENSP00000456201.1:p.Gly373Arg
ENST00000611258.4:c.1117G>C	ENSP00000481090.1:p.Gly373Arg
NM_001178098.1:c.1117G>C	NP_001171569.1:p.Gly373Arg
NM_001770.5:c.1117G>C , LRG_35t1:c.1117G>C	NP_001761.3:p.Gly373Arg
XM_006721103.2:c.850G>C	XP_006721166.1:p.Gly284Arg
XR_950871.1:n.1130G>C
XR_950872.1:n.1019G>C
XM_006721103.3:c.850G>C	XP_006721166.1:p.Gly284Arg
XM_017023893.1:c.850G>C	XP_016879382.1:p.Gly284Arg
XR_950871.2:n.1113G>C
NM_001178098.2:c.1117G>C	NP_001171569.1:p.Gly373Arg
NM_001770.6:c.1117G>C MANE Select	NP_001761.3:p.Gly373Arg
NM_001385732.1:c.850G>C	NP_001372661.1:p.Gly284Arg
NR_169755.1:n.1459G>C