Canonical Allele Identifier: CA395406488

Gene: CD19

Linked Data

• MyVariant Identifiers: chr16:g.28948842A>C (hg19) ; chr16:g.28937521A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937521A>C , CM000678.2:g.28937521A>C	GRCh38
NC_000016.9:g.28948842A>C , CM000678.1:g.28948842A>C	GRCh37
NC_000016.8:g.28856343A>C	NCBI36
NG_007275.1:g.10583A>C , LRG_35:g.10583A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1370A>C	ENSP00000313419.4:p.Asn457Thr
ENST00000538922.8:c.1370A>C MANE Select	ENSP00000437940.2:p.Asn457Thr
ENST00000324662.7:c.1370A>C	ENSP00000313419.3:p.Asn457Thr
ENST00000538922.5:c.1370A>C	ENSP00000437940.1:p.Asn457Thr
ENST00000565089.5:n.1704A>C
ENST00000567368.1:n.510A>C
ENST00000567541.5:c.1370A>C	ENSP00000456201.1:p.Asn457Thr
ENST00000611258.4:c.1369A>C	ENSP00000481090.1:p.Thr457Pro
NM_001178098.1:c.1370A>C	NP_001171569.1:p.Asn457Thr
NM_001770.5:c.1370A>C , LRG_35t1:c.1370A>C	NP_001761.3:p.Asn457Thr
XM_006721103.2:c.1103A>C	XP_006721166.1:p.Asn368Thr
XM_006721103.3:c.1103A>C	XP_006721166.1:p.Asn368Thr
XM_017023893.1:c.1103A>C	XP_016879382.1:p.Asn368Thr
NM_001178098.2:c.1370A>C	NP_001171569.1:p.Asn457Thr
NM_001770.6:c.1370A>C MANE Select	NP_001761.3:p.Asn457Thr
NM_001385732.1:c.1103A>C	NP_001372661.1:p.Asn368Thr
NR_169755.1:n.1712A>C