Canonical Allele Identifier: CA494489849

Gene: CD19

Linked Data

• dbSNP Id: rs1964811809
• MyVariant Identifiers: chr16:g.28949094C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937773C>T , CM000678.2:g.28937773C>T	GRCh38
NC_000016.9:g.28949094C>T , CM000678.1:g.28949094C>T	GRCh37
NC_000016.8:g.28856595C>T	NCBI36
NG_007275.1:g.10835C>T , LRG_35:g.10835C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1434C>T	ENSP00000313419.4:p.Phe478=
ENST00000538922.8:c.1434C>T MANE Select	ENSP00000437940.2:p.Phe478=
ENST00000324662.7:c.1434C>T	ENSP00000313419.3:p.Phe478=
ENST00000538922.5:c.1434C>T	ENSP00000437940.1:p.Phe478=
ENST00000565089.5:n.1868C>T
ENST00000567368.1:n.569+93C>T
ENST00000567541.5:c.1434C>T	ENSP00000456201.1:p.Phe478=
ENST00000611258.4:c.*29C>T	ENSP00000481090.1:n.*29C>T
NM_001178098.1:c.1434C>T	NP_001171569.1:p.Phe478=
NM_001770.5:c.1434C>T , LRG_35t1:c.1434C>T	NP_001761.3:p.Phe478=
XM_006721103.2:c.1167C>T	XP_006721166.1:p.Phe389=
XM_006721103.3:c.1167C>T	XP_006721166.1:p.Phe389=
XM_017023893.1:c.1167C>T	XP_016879382.1:p.Phe389=
NM_001178098.2:c.1434C>T	NP_001171569.1:p.Phe478=
NM_001770.6:c.1434C>T MANE Select	NP_001761.3:p.Phe478=
NM_001385732.1:c.1167C>T	NP_001372661.1:p.Phe389=
NR_169755.1:n.1776C>T