Canonical Allele Identifier: CA7988706

Gene: CD19

Linked Data

• dbSNP Id: rs762628877
• ExAC: 16:28949160 T / C
• gnomAD v2: 16-28949160-T-C
• gnomAD v4: 16-28937839-T-C
• MyVariant Identifiers: chr16:g.28949160T>C (hg19) ; chr16:g.28937839T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937839T>C , CM000678.2:g.28937839T>C	GRCh38
NC_000016.9:g.28949160T>C , CM000678.1:g.28949160T>C	GRCh37
NC_000016.8:g.28856661T>C	NCBI36
NG_007275.1:g.10901T>C , LRG_35:g.10901T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1486+14T>C	ENSP00000313419.4:n.1486+14T>C
ENST00000538922.8:c.1486+14T>C MANE Select	ENSP00000437940.2:n.1486+14T>C
ENST00000324662.7:c.1486+14T>C	ENSP00000313419.3:n.1486+14T>C
ENST00000538922.5:c.1486+14T>C	ENSP00000437940.1:n.1486+14T>C
ENST00000565089.5:n.1920+14T>C
ENST00000567368.1:n.569+159T>C
ENST00000567541.5:c.1486+14T>C	ENSP00000456201.1:n.1486+14T>C
ENST00000611258.4:c.*81+14T>C	ENSP00000481090.1:n.*81+14T>C
NM_001178098.1:c.1486+14T>C	NP_001171569.1:n.1486+14T>C
NM_001770.5:c.1486+14T>C , LRG_35t1:c.1486+14T>C	NP_001761.3:n.1486+14T>C
XM_006721103.2:c.1219+14T>C	XP_006721166.1:n.1219+14T>C
XM_006721103.3:c.1219+14T>C	XP_006721166.1:n.1219+14T>C
XM_017023893.1:c.1219+14T>C	XP_016879382.1:n.1219+14T>C
NM_001178098.2:c.1486+14T>C	NP_001171569.1:n.1486+14T>C
NM_001770.6:c.1486+14T>C MANE Select	NP_001761.3:n.1486+14T>C
NM_001385732.1:c.1219+14T>C	NP_001372661.1:n.1219+14T>C
NR_169755.1:n.1828+14T>C