Canonical Allele Identifier: CA395405512

Gene: CD19

Linked Data

• gnomAD v4: 16-28937038-G-T
• COSMIC: COSM6318911
• MyVariant Identifiers: chr16:g.28948359G>T (hg19) ; chr16:g.28937038G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937038G>T , CM000678.2:g.28937038G>T	GRCh38
NC_000016.9:g.28948359G>T , CM000678.1:g.28948359G>T	GRCh37
NC_000016.8:g.28855860G>T	NCBI36
NG_007275.1:g.10100G>T , LRG_35:g.10100G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1100G>T	ENSP00000313419.4:p.Trp367Leu
ENST00000538922.8:c.1100G>T MANE Select	ENSP00000437940.2:p.Trp367Leu
ENST00000324662.7:c.1100G>T	ENSP00000313419.3:p.Trp367Leu
ENST00000538922.5:c.1100G>T	ENSP00000437940.1:p.Trp367Leu
ENST00000565089.5:n.1434G>T
ENST00000567368.1:n.240G>T
ENST00000567541.5:c.1100G>T	ENSP00000456201.1:p.Trp367Leu
ENST00000611258.4:c.1100G>T	ENSP00000481090.1:p.Trp367Leu
NM_001178098.1:c.1100G>T	NP_001171569.1:p.Trp367Leu
NM_001770.5:c.1100G>T , LRG_35t1:c.1100G>T	NP_001761.3:p.Trp367Leu
XM_006721103.2:c.833G>T	XP_006721166.1:p.Trp278Leu
XR_950871.1:n.1113G>T
XR_950872.1:n.1002G>T
XM_006721103.3:c.833G>T	XP_006721166.1:p.Trp278Leu
XM_017023893.1:c.833G>T	XP_016879382.1:p.Trp278Leu
XR_950871.2:n.1096G>T
NM_001178098.2:c.1100G>T	NP_001171569.1:p.Trp367Leu
NM_001770.6:c.1100G>T MANE Select	NP_001761.3:p.Trp367Leu
NM_001385732.1:c.833G>T	NP_001372661.1:p.Trp278Leu
NR_169755.1:n.1442G>T