Canonical Allele Identifier: CA2215894738
Gene: CD19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28937451C= , CM000678.2:g.28937451C= GRCh38
NC_000016.9:g.28948772C= , CM000678.1:g.28948772C= GRCh37
NC_000016.8:g.28856273C= NCBI36
NG_007275.1:g.10513C= , LRG_35:g.10513C=

Transcript Alleles

HGVS Amino-acid change
ENST00000324662.8:c.1304-4C= ENSP00000313419.4:n.1304-4C=
ENST00000538922.8:c.1304-4C= MANE Select ENSP00000437940.2:n.1304-4C=
ENST00000324662.7:c.1304-4C= ENSP00000313419.3:n.1304-4C=
ENST00000538922.5:c.1304-4C= ENSP00000437940.1:n.1304-4C=
ENST00000565089.5:n.1638-4C=
ENST00000567368.1:n.444-4C=
ENST00000567541.5:c.1304-4C= ENSP00000456201.1:n.1304-4C=
ENST00000611258.4:c.1303-4C= ENSP00000481090.1:n.1303-4C=
NM_001178098.1:c.1304-4C= NP_001171569.1:n.1304-4C=
NM_001770.5:c.1304-4C= , LRG_35t1:c.1304-4C= NP_001761.3:n.1304-4C=
XM_006721103.2:c.1037-4C= XP_006721166.1:n.1037-4C=
XM_006721103.3:c.1037-4C= XP_006721166.1:n.1037-4C=
XM_017023893.1:c.1037-4C= XP_016879382.1:n.1037-4C=
NM_001178098.2:c.1304-4C= NP_001171569.1:n.1304-4C=
NM_001770.6:c.1304-4C= MANE Select NP_001761.3:n.1304-4C=
NM_001385732.1:c.1037-4C= NP_001372661.1:n.1037-4C=
NR_169755.1:n.1646-4C=