Canonical Allele Identifier: CA279220178

Gene: CD19

Linked Data

• ClinVar Variation Id: 3005761
• ClinVar RCV Id: RCV003863848
• dbSNP Id: rs966035942
• gnomAD v3: 16-28937027-C-T
• gnomAD v4: 16-28937027-C-T
• MyVariant Identifiers: chr16:g.28948348C>T (hg19) ; chr16:g.28937027C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937027C>T , CM000678.2:g.28937027C>T	GRCh38
NC_000016.9:g.28948348C>T , CM000678.1:g.28948348C>T	GRCh37
NC_000016.8:g.28855849C>T	NCBI36
NG_007275.1:g.10089C>T , LRG_35:g.10089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1089C>T	ENSP00000313419.4:p.Arg363=
ENST00000538922.8:c.1089C>T MANE Select	ENSP00000437940.2:p.Arg363=
ENST00000324662.7:c.1089C>T	ENSP00000313419.3:p.Arg363=
ENST00000538922.5:c.1089C>T	ENSP00000437940.1:p.Arg363=
ENST00000565089.5:n.1423C>T
ENST00000567368.1:n.229C>T
ENST00000567541.5:c.1089C>T	ENSP00000456201.1:p.Arg363=
ENST00000611258.4:c.1089C>T	ENSP00000481090.1:p.Arg363=
NM_001178098.1:c.1089C>T	NP_001171569.1:p.Arg363=
NM_001770.5:c.1089C>T , LRG_35t1:c.1089C>T	NP_001761.3:p.Arg363=
XM_006721103.2:c.822C>T	XP_006721166.1:p.Arg274=
XR_950871.1:n.1102C>T
XR_950872.1:n.991C>T
XM_006721103.3:c.822C>T	XP_006721166.1:p.Arg274=
XM_017023893.1:c.822C>T	XP_016879382.1:p.Arg274=
XR_950871.2:n.1085C>T
NM_001178098.2:c.1089C>T	NP_001171569.1:p.Arg363=
NM_001770.6:c.1089C>T MANE Select	NP_001761.3:p.Arg363=
NM_001385732.1:c.822C>T	NP_001372661.1:p.Arg274=
NR_169755.1:n.1431C>T