Canonical Allele Identifier: CA395406338

Gene: CD19

Linked Data

• MyVariant Identifiers: chr16:g.28948786C>A (hg19) ; chr16:g.28937465C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937465C>A , CM000678.2:g.28937465C>A	GRCh38
NC_000016.9:g.28948786C>A , CM000678.1:g.28948786C>A	GRCh37
NC_000016.8:g.28856287C>A	NCBI36
NG_007275.1:g.10527C>A , LRG_35:g.10527C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1314C>A	ENSP00000313419.4:p.Gly438=
ENST00000538922.8:c.1314C>A MANE Select	ENSP00000437940.2:p.Gly438=
ENST00000324662.7:c.1314C>A	ENSP00000313419.3:p.Gly438=
ENST00000538922.5:c.1314C>A	ENSP00000437940.1:p.Gly438=
ENST00000565089.5:n.1648C>A
ENST00000567368.1:n.454C>A
ENST00000567541.5:c.1314C>A	ENSP00000456201.1:p.Gly438=
ENST00000611258.4:c.1313C>A	ENSP00000481090.1:p.Ala438Asp
NM_001178098.1:c.1314C>A	NP_001171569.1:p.Gly438=
NM_001770.5:c.1314C>A , LRG_35t1:c.1314C>A	NP_001761.3:p.Gly438=
XM_006721103.2:c.1047C>A	XP_006721166.1:p.Gly349=
XM_006721103.3:c.1047C>A	XP_006721166.1:p.Gly349=
XM_017023893.1:c.1047C>A	XP_016879382.1:p.Gly349=
NM_001178098.2:c.1314C>A	NP_001171569.1:p.Gly438=
NM_001770.6:c.1314C>A MANE Select	NP_001761.3:p.Gly438=
NM_001385732.1:c.1047C>A	NP_001372661.1:p.Gly349=
NR_169755.1:n.1656C>A