Canonical Allele Identifier: CA7988650

Gene: CD19

Linked Data

• dbSNP Id: rs778904923
• ExAC: 16:28948876 C / T
• gnomAD v2: 16-28948876-C-T
• gnomAD v4: 16-28937555-C-T
• MyVariant Identifiers: chr16:g.28948876C>T (hg19) ; chr16:g.28937555C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937555C>T , CM000678.2:g.28937555C>T	GRCh38
NC_000016.9:g.28948876C>T , CM000678.1:g.28948876C>T	GRCh37
NC_000016.8:g.28856377C>T	NCBI36
NG_007275.1:g.10617C>T , LRG_35:g.10617C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324662.8:c.1372+32C>T	ENSP00000313419.4:n.1372+32C>T
ENST00000538922.8:c.1372+32C>T MANE Select	ENSP00000437940.2:n.1372+32C>T
ENST00000324662.7:c.1372+32C>T	ENSP00000313419.3:n.1372+32C>T
ENST00000538922.5:c.1372+32C>T	ENSP00000437940.1:n.1372+32C>T
ENST00000565089.5:n.1738C>T
ENST00000567368.1:n.512+32C>T
ENST00000567541.5:c.1372+32C>T	ENSP00000456201.1:n.1372+32C>T
ENST00000611258.4:c.1371+32C>T	ENSP00000481090.1:n.1371+32C>T
NM_001178098.1:c.1372+32C>T	NP_001171569.1:n.1372+32C>T
NM_001770.5:c.1372+32C>T , LRG_35t1:c.1372+32C>T	NP_001761.3:n.1372+32C>T
XM_006721103.2:c.1105+32C>T	XP_006721166.1:n.1105+32C>T
XM_006721103.3:c.1105+32C>T	XP_006721166.1:n.1105+32C>T
XM_017023893.1:c.1105+32C>T	XP_016879382.1:n.1105+32C>T
NM_001178098.2:c.1372+32C>T	NP_001171569.1:n.1372+32C>T
NM_001770.6:c.1372+32C>T MANE Select	NP_001761.3:n.1372+32C>T
NM_001385732.1:c.1105+32C>T	NP_001372661.1:n.1105+32C>T
NR_169755.1:n.1714+32C>T