Canonical Allele Identifier: CA2215894681

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937346C= , CM000678.2:g.28937346C=	GRCh38
NC_000016.9:g.28948667C= , CM000678.1:g.28948667C=	GRCh37
NC_000016.8:g.28856168C=	NCBI36
NG_007275.1:g.10408C= , LRG_35:g.10408C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1274C=	ENSP00000313419.4:p.Ser425=
ENST00000538922.8:c.1274C= MANE Select	ENSP00000437940.2:p.Ser425=
ENST00000324662.7:c.1274C=	ENSP00000313419.3:p.Ser425=
ENST00000538922.5:c.1274C=	ENSP00000437940.1:p.Ser425=
ENST00000565089.5:n.1608C=
ENST00000567368.1:n.414C=
ENST00000567541.5:c.1274C=	ENSP00000456201.1:p.Ser425=
ENST00000611258.4:c.1273C=	ENSP00000481090.1:p.Pro425=
NM_001178098.1:c.1274C=	NP_001171569.1:p.Ser425=
NM_001770.5:c.1274C= , LRG_35t1:c.1274C=	NP_001761.3:p.Ser425=
XM_006721103.2:c.1007C=	XP_006721166.1:p.Ser336=
XM_006721103.3:c.1007C=	XP_006721166.1:p.Ser336=
XM_017023893.1:c.1007C=	XP_016879382.1:p.Ser336=
NM_001178098.2:c.1274C=	NP_001171569.1:p.Ser425=
NM_001770.6:c.1274C= MANE Select	NP_001761.3:p.Ser425=
NM_001385732.1:c.1007C=	NP_001372661.1:p.Ser336=
NR_169755.1:n.1616C=