Canonical Allele Identifier: CA494489856

Gene: CD19

Linked Data

• MyVariant Identifiers: chr16:g.28949103T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937782T>G , CM000678.2:g.28937782T>G	GRCh38
NC_000016.9:g.28949103T>G , CM000678.1:g.28949103T>G	GRCh37
NC_000016.8:g.28856604T>G	NCBI36
NG_007275.1:g.10844T>G , LRG_35:g.10844T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1443T>G	ENSP00000313419.4:p.Pro481=
ENST00000538922.8:c.1443T>G MANE Select	ENSP00000437940.2:p.Pro481=
ENST00000324662.7:c.1443T>G	ENSP00000313419.3:p.Pro481=
ENST00000538922.5:c.1443T>G	ENSP00000437940.1:p.Pro481=
ENST00000565089.5:n.1877T>G
ENST00000567368.1:n.569+102T>G
ENST00000567541.5:c.1443T>G	ENSP00000456201.1:p.Pro481=
ENST00000611258.4:c.*38T>G	ENSP00000481090.1:n.*38T>G
NM_001178098.1:c.1443T>G	NP_001171569.1:p.Pro481=
NM_001770.5:c.1443T>G , LRG_35t1:c.1443T>G	NP_001761.3:p.Pro481=
XM_006721103.2:c.1176T>G	XP_006721166.1:p.Pro392=
XM_006721103.3:c.1176T>G	XP_006721166.1:p.Pro392=
XM_017023893.1:c.1176T>G	XP_016879382.1:p.Pro392=
NM_001178098.2:c.1443T>G	NP_001171569.1:p.Pro481=
NM_001770.6:c.1443T>G MANE Select	NP_001761.3:p.Pro481=
NM_001385732.1:c.1176T>G	NP_001372661.1:p.Pro392=
NR_169755.1:n.1785T>G