Canonical Allele Identifier: CA2215894495
Gene: CD19 HGNC NCBI

Linked Data

dbSNP Id: rs1964787321

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28937000T>C , CM000678.2:g.28937000T>C GRCh38
NC_000016.9:g.28948321T>C , CM000678.1:g.28948321T>C GRCh37
NC_000016.8:g.28855822T>C NCBI36
NG_007275.1:g.10062T>C , LRG_35:g.10062T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324662.8:c.1085-23T>C ENSP00000313419.4:n.1085-23T>C
ENST00000538922.8:c.1085-23T>C MANE Select ENSP00000437940.2:n.1085-23T>C
ENST00000324662.7:c.1085-23T>C ENSP00000313419.3:n.1085-23T>C
ENST00000538922.5:c.1085-23T>C ENSP00000437940.1:n.1085-23T>C
ENST00000565089.5:n.1419-23T>C
ENST00000567368.1:n.202T>C
ENST00000567541.5:c.1085-23T>C ENSP00000456201.1:n.1085-23T>C
ENST00000611258.4:c.1085-23T>C ENSP00000481090.1:n.1085-23T>C
NM_001178098.1:c.1085-23T>C NP_001171569.1:n.1085-23T>C
NM_001770.5:c.1085-23T>C , LRG_35t1:c.1085-23T>C NP_001761.3:n.1085-23T>C
XM_006721103.2:c.818-23T>C XP_006721166.1:n.818-23T>C
XR_950871.1:n.1098-23T>C
XR_950872.1:n.987-23T>C
XM_006721103.3:c.818-23T>C XP_006721166.1:n.818-23T>C
XM_017023893.1:c.818-23T>C XP_016879382.1:n.818-23T>C
XR_950871.2:n.1081-23T>C
NM_001178098.2:c.1085-23T>C NP_001171569.1:n.1085-23T>C
NM_001770.6:c.1085-23T>C MANE Select NP_001761.3:n.1085-23T>C
NM_001385732.1:c.818-23T>C NP_001372661.1:n.818-23T>C
NR_169755.1:n.1427-23T>C