Canonical Allele Identifier: CA719706643

Gene: CD19

Linked Data

• dbSNP Id: rs1383832970
• MyVariant Identifiers: chr16:g.28948496_28948497del (hg19) ; chr16:g.28937175_28937176del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937176_28937177del , CM000678.2:g.28937176_28937177del	GRCh38
NC_000016.9:g.28948497_28948498del , CM000678.1:g.28948497_28948498del	GRCh37
NC_000016.8:g.28855998_28855999del	NCBI36
NG_007275.1:g.10238_10239del , LRG_35:g.10238_10239del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1198+40_1198+41del	ENSP00000313419.4:n.1198+40_1198+41del
ENST00000538922.8:c.1198+40_1198+41del MANE Select	ENSP00000437940.2:n.1198+40_1198+41del
ENST00000324662.7:c.1198+40_1198+41del	ENSP00000313419.3:n.1198+40_1198+41del
ENST00000538922.5:c.1198+40_1198+41del	ENSP00000437940.1:n.1198+40_1198+41del
ENST00000565089.5:n.1532+40_1532+41del
ENST00000567368.1:n.338+40_338+41del
ENST00000567541.5:c.1198+40_1198+41del	ENSP00000456201.1:n.1198+40_1198+41del
ENST00000611258.4:c.1197+40_1197+41del	ENSP00000481090.1:n.1197+40_1197+41del
NM_001178098.1:c.1198+40_1198+41del	NP_001171569.1:n.1198+40_1198+41del
NM_001770.5:c.1198+40_1198+41del , LRG_35t1:c.1198+40_1198+41del	NP_001761.3:n.1198+40_1198+41del
XM_006721103.2:c.931+40_931+41del	XP_006721166.1:n.931+40_931+41del
XM_006721103.3:c.931+40_931+41del	XP_006721166.1:n.931+40_931+41del
XM_017023893.1:c.931+40_931+41del	XP_016879382.1:n.931+40_931+41del
NM_001178098.2:c.1198+40_1198+41del	NP_001171569.1:n.1198+40_1198+41del
NM_001770.6:c.1198+40_1198+41del MANE Select	NP_001761.3:n.1198+40_1198+41del
NM_001385732.1:c.931+40_931+41del	NP_001372661.1:n.931+40_931+41del
NR_169755.1:n.1540+40_1540+41del