Canonical Allele Identifier: CA2215894901

Gene: CD19

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937800C= , CM000678.2:g.28937800C=	GRCh38
NC_000016.9:g.28949121C= , CM000678.1:g.28949121C=	GRCh37
NC_000016.8:g.28856622C=	NCBI36
NG_007275.1:g.10862C= , LRG_35:g.10862C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1461C=	ENSP00000313419.4:p.Asp487=
ENST00000538922.8:c.1461C= MANE Select	ENSP00000437940.2:p.Asp487=
ENST00000324662.7:c.1461C=	ENSP00000313419.3:p.Asp487=
ENST00000538922.5:c.1461C=	ENSP00000437940.1:p.Asp487=
ENST00000565089.5:n.1895C=
ENST00000567368.1:n.569+120C=
ENST00000567541.5:c.1461C=	ENSP00000456201.1:p.Asp487=
ENST00000611258.4:c.*56C=	ENSP00000481090.1:n.*56C=
NM_001178098.1:c.1461C=	NP_001171569.1:p.Asp487=
NM_001770.5:c.1461C= , LRG_35t1:c.1461C=	NP_001761.3:p.Asp487=
XM_006721103.2:c.1194C=	XP_006721166.1:p.Asp398=
XM_006721103.3:c.1194C=	XP_006721166.1:p.Asp398=
XM_017023893.1:c.1194C=	XP_016879382.1:p.Asp398=
NM_001178098.2:c.1461C=	NP_001171569.1:p.Asp487=
NM_001770.6:c.1461C= MANE Select	NP_001761.3:p.Asp487=
NM_001385732.1:c.1194C=	NP_001372661.1:p.Asp398=
NR_169755.1:n.1803C=