Canonical Allele Identifier: CA2215894830

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937648A= , CM000678.2:g.28937648A=	GRCh38
NC_000016.9:g.28948969A= , CM000678.1:g.28948969A=	GRCh37
NC_000016.8:g.28856470A=	NCBI36
NG_007275.1:g.10710A= , LRG_35:g.10710A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1397A=	ENSP00000313419.4:p.Glu466=
ENST00000538922.8:c.1397A= MANE Select	ENSP00000437940.2:p.Glu466=
ENST00000324662.7:c.1397A=	ENSP00000313419.3:p.Glu466=
ENST00000538922.5:c.1397A=	ENSP00000437940.1:p.Glu466=
ENST00000565089.5:n.1831A=
ENST00000567368.1:n.537A=
ENST00000567541.5:c.1397A=	ENSP00000456201.1:p.Glu466=
ENST00000611258.4:c.1396A=	ENSP00000481090.1:p.Lys466=
NM_001178098.1:c.1397A=	NP_001171569.1:p.Glu466=
NM_001770.5:c.1397A= , LRG_35t1:c.1397A=	NP_001761.3:p.Glu466=
XM_006721103.2:c.1130A=	XP_006721166.1:p.Glu377=
XM_006721103.3:c.1130A=	XP_006721166.1:p.Glu377=
XM_017023893.1:c.1130A=	XP_016879382.1:p.Glu377=
NM_001178098.2:c.1397A=	NP_001171569.1:p.Glu466=
NM_001770.6:c.1397A= MANE Select	NP_001761.3:p.Glu466=
NM_001385732.1:c.1130A=	NP_001372661.1:p.Glu377=
NR_169755.1:n.1739A=