Canonical Allele Identifier: CA395405539
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047131
ClinVar RCV Id: RCV001351799
dbSNP Id: rs1964789310

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28937043G>A , CM000678.2:g.28937043G>A GRCh38
NC_000016.9:g.28948364G>A , CM000678.1:g.28948364G>A GRCh37
NC_000016.8:g.28855865G>A NCBI36
NG_007275.1:g.10105G>A , LRG_35:g.10105G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324662.8:c.1105G>A ENSP00000313419.4:p.Ala369Thr
ENST00000538922.8:c.1105G>A MANE Select ENSP00000437940.2:p.Ala369Thr
ENST00000324662.7:c.1105G>A ENSP00000313419.3:p.Ala369Thr
ENST00000538922.5:c.1105G>A ENSP00000437940.1:p.Ala369Thr
ENST00000565089.5:n.1439G>A
ENST00000567368.1:n.245G>A
ENST00000567541.5:c.1105G>A ENSP00000456201.1:p.Ala369Thr
ENST00000611258.4:c.1105G>A ENSP00000481090.1:p.Ala369Thr
NM_001178098.1:c.1105G>A NP_001171569.1:p.Ala369Thr
NM_001770.5:c.1105G>A , LRG_35t1:c.1105G>A NP_001761.3:p.Ala369Thr
XM_006721103.2:c.838G>A XP_006721166.1:p.Ala280Thr
XR_950871.1:n.1118G>A
XR_950872.1:n.1007G>A
XM_006721103.3:c.838G>A XP_006721166.1:p.Ala280Thr
XM_017023893.1:c.838G>A XP_016879382.1:p.Ala280Thr
XR_950871.2:n.1101G>A
NM_001178098.2:c.1105G>A NP_001171569.1:p.Ala369Thr
NM_001770.6:c.1105G>A MANE Select NP_001761.3:p.Ala369Thr
NM_001385732.1:c.838G>A NP_001372661.1:p.Ala280Thr
NR_169755.1:n.1447G>A