Canonical Allele Identifier: CA395405986

Gene: CD19

Linked Data

• MyVariant Identifiers: chr16:g.28948594C>A (hg19) ; chr16:g.28937273C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937273C>A , CM000678.2:g.28937273C>A	GRCh38
NC_000016.9:g.28948594C>A , CM000678.1:g.28948594C>A	GRCh37
NC_000016.8:g.28856095C>A	NCBI36
NG_007275.1:g.10335C>A , LRG_35:g.10335C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1201C>A	ENSP00000313419.4:p.Pro401Thr
ENST00000538922.8:c.1201C>A MANE Select	ENSP00000437940.2:p.Pro401Thr
ENST00000324662.7:c.1201C>A	ENSP00000313419.3:p.Pro401Thr
ENST00000538922.5:c.1201C>A	ENSP00000437940.1:p.Pro401Thr
ENST00000565089.5:n.1535C>A
ENST00000567368.1:n.341C>A
ENST00000567541.5:c.1201C>A	ENSP00000456201.1:p.Pro401Thr
ENST00000611258.4:c.1200C>A	ENSP00000481090.1:p.Ala400=
NM_001178098.1:c.1201C>A	NP_001171569.1:p.Pro401Thr
NM_001770.5:c.1201C>A , LRG_35t1:c.1201C>A	NP_001761.3:p.Pro401Thr
XM_006721103.2:c.934C>A	XP_006721166.1:p.Pro312Thr
XM_006721103.3:c.934C>A	XP_006721166.1:p.Pro312Thr
XM_017023893.1:c.934C>A	XP_016879382.1:p.Pro312Thr
NM_001178098.2:c.1201C>A	NP_001171569.1:p.Pro401Thr
NM_001770.6:c.1201C>A MANE Select	NP_001761.3:p.Pro401Thr
NM_001385732.1:c.934C>A	NP_001372661.1:p.Pro312Thr
NR_169755.1:n.1543C>A