Canonical Allele Identifier: CA16620185
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 421012
ClinVar RCV Id: RCV000480690
dbSNP Id: rs1064794850

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28937524G>A , CM000678.2:g.28937524G>A GRCh38
NC_000016.9:g.28948845G>A , CM000678.1:g.28948845G>A GRCh37
NC_000016.8:g.28856346G>A NCBI36
NG_007275.1:g.10586G>A , LRG_35:g.10586G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000324662.8:c.1372+1G>A ENSP00000313419.4:n.1372+1G>A
ENST00000538922.8:c.1372+1G>A MANE Select ENSP00000437940.2:n.1372+1G>A
ENST00000324662.7:c.1372+1G>A ENSP00000313419.3:n.1372+1G>A
ENST00000538922.5:c.1372+1G>A ENSP00000437940.1:n.1372+1G>A
ENST00000565089.5:n.1707G>A
ENST00000567368.1:n.512+1G>A
ENST00000567541.5:c.1372+1G>A ENSP00000456201.1:n.1372+1G>A
ENST00000611258.4:c.1371+1G>A ENSP00000481090.1:n.1371+1G>A
NM_001178098.1:c.1372+1G>A NP_001171569.1:n.1372+1G>A
NM_001770.5:c.1372+1G>A , LRG_35t1:c.1372+1G>A NP_001761.3:n.1372+1G>A
XM_006721103.2:c.1105+1G>A XP_006721166.1:n.1105+1G>A
XM_006721103.3:c.1105+1G>A XP_006721166.1:n.1105+1G>A
XM_017023893.1:c.1105+1G>A XP_016879382.1:n.1105+1G>A
NM_001178098.2:c.1372+1G>A NP_001171569.1:n.1372+1G>A
NM_001770.6:c.1372+1G>A MANE Select NP_001761.3:n.1372+1G>A
NM_001385732.1:c.1105+1G>A NP_001372661.1:n.1105+1G>A
NR_169755.1:n.1714+1G>A