Canonical Allele Identifier: CA395406369

Gene: CD19

Linked Data

• gnomAD v4: 16-28937477-T-C
• MyVariant Identifiers: chr16:g.28948798T>C (hg19) ; chr16:g.28937477T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937477T>C , CM000678.2:g.28937477T>C	GRCh38
NC_000016.9:g.28948798T>C , CM000678.1:g.28948798T>C	GRCh37
NC_000016.8:g.28856299T>C	NCBI36
NG_007275.1:g.10539T>C , LRG_35:g.10539T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1326T>C	ENSP00000313419.4:p.Pro442=
ENST00000538922.8:c.1326T>C MANE Select	ENSP00000437940.2:p.Pro442=
ENST00000324662.7:c.1326T>C	ENSP00000313419.3:p.Pro442=
ENST00000538922.5:c.1326T>C	ENSP00000437940.1:p.Pro442=
ENST00000565089.5:n.1660T>C
ENST00000567368.1:n.466T>C
ENST00000567541.5:c.1326T>C	ENSP00000456201.1:p.Pro442=
ENST00000611258.4:c.1325T>C	ENSP00000481090.1:p.Leu442Pro
NM_001178098.1:c.1326T>C	NP_001171569.1:p.Pro442=
NM_001770.5:c.1326T>C , LRG_35t1:c.1326T>C	NP_001761.3:p.Pro442=
XM_006721103.2:c.1059T>C	XP_006721166.1:p.Pro353=
XM_006721103.3:c.1059T>C	XP_006721166.1:p.Pro353=
XM_017023893.1:c.1059T>C	XP_016879382.1:p.Pro353=
NM_001178098.2:c.1326T>C	NP_001171569.1:p.Pro442=
NM_001770.6:c.1326T>C MANE Select	NP_001761.3:p.Pro442=
NM_001385732.1:c.1059T>C	NP_001372661.1:p.Pro353=
NR_169755.1:n.1668T>C