Canonical Allele Identifier: CA2632553476

Gene: CD19

Linked Data

• gnomAD v4: 16-28937435-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937435C>T , CM000678.2:g.28937435C>T	GRCh38
NC_000016.9:g.28948756C>T , CM000678.1:g.28948756C>T	GRCh37
NC_000016.8:g.28856257C>T	NCBI36
NG_007275.1:g.10497C>T , LRG_35:g.10497C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324662.8:c.1304-20C>T	ENSP00000313419.4:n.1304-20C>T
ENST00000538922.8:c.1304-20C>T MANE Select	ENSP00000437940.2:n.1304-20C>T
ENST00000324662.7:c.1304-20C>T	ENSP00000313419.3:n.1304-20C>T
ENST00000538922.5:c.1304-20C>T	ENSP00000437940.1:n.1304-20C>T
ENST00000565089.5:n.1638-20C>T
ENST00000567368.1:n.444-20C>T
ENST00000567541.5:c.1304-20C>T	ENSP00000456201.1:n.1304-20C>T
ENST00000611258.4:c.1303-20C>T	ENSP00000481090.1:n.1303-20C>T
NM_001178098.1:c.1304-20C>T	NP_001171569.1:n.1304-20C>T
NM_001770.5:c.1304-20C>T , LRG_35t1:c.1304-20C>T	NP_001761.3:n.1304-20C>T
XM_006721103.2:c.1037-20C>T	XP_006721166.1:n.1037-20C>T
XM_006721103.3:c.1037-20C>T	XP_006721166.1:n.1037-20C>T
XM_017023893.1:c.1037-20C>T	XP_016879382.1:n.1037-20C>T
NM_001178098.2:c.1304-20C>T	NP_001171569.1:n.1304-20C>T
NM_001770.6:c.1304-20C>T MANE Select	NP_001761.3:n.1304-20C>T
NM_001385732.1:c.1037-20C>T	NP_001372661.1:n.1037-20C>T
NR_169755.1:n.1646-20C>T