Canonical Allele Identifier: CA395406648

Gene: CD19

Linked Data

• dbSNP Id: rs375572262
• MyVariant Identifiers: chr16:g.28948980C>T (hg19) ; chr16:g.28937659C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28937659C>T , CM000678.2:g.28937659C>T	GRCh38
NC_000016.9:g.28948980C>T , CM000678.1:g.28948980C>T	GRCh37
NC_000016.8:g.28856481C>T	NCBI36
NG_007275.1:g.10721C>T , LRG_35:g.10721C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324662.8:c.1408C>T	ENSP00000313419.4:p.Gln470Ter
ENST00000538922.8:c.1408C>T MANE Select	ENSP00000437940.2:p.Gln470Ter
ENST00000324662.7:c.1408C>T	ENSP00000313419.3:p.Gln470Ter
ENST00000538922.5:c.1408C>T	ENSP00000437940.1:p.Gln470Ter
ENST00000565089.5:n.1842C>T
ENST00000567368.1:n.548C>T
ENST00000567541.5:c.1408C>T	ENSP00000456201.1:p.Gln470Ter
ENST00000611258.4:c.*3C>T	ENSP00000481090.1:n.*3C>T
NM_001178098.1:c.1408C>T	NP_001171569.1:p.Gln470Ter
NM_001770.5:c.1408C>T , LRG_35t1:c.1408C>T	NP_001761.3:p.Gln470Ter
XM_006721103.2:c.1141C>T	XP_006721166.1:p.Gln381Ter
XM_006721103.3:c.1141C>T	XP_006721166.1:p.Gln381Ter
XM_017023893.1:c.1141C>T	XP_016879382.1:p.Gln381Ter
NM_001178098.2:c.1408C>T	NP_001171569.1:p.Gln470Ter
NM_001770.6:c.1408C>T MANE Select	NP_001761.3:p.Gln470Ter
NM_001385732.1:c.1141C>T	NP_001372661.1:p.Gln381Ter
NR_169755.1:n.1750C>T