Canonical Allele Identifier: CA9264481

Gene: BRD4

Linked Data

• ClinVar Variation Id: 710756
• ClinVar RCV Id: RCV000882400 ; RCV003940450
• dbSNP Id: rs61740415
• ExAC: 19:15349647 G / A
• gnomAD v2: 19-15349647-G-A
• gnomAD v3: 19-15238836-G-A
• gnomAD v4: 19-15238836-G-A
• MyVariant Identifiers: chr19:g.15349647G>A (hg19) ; chr19:g.15238836G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15238836G>A , CM000681.2:g.15238836G>A	GRCh38
NC_000019.9:g.15349647G>A , CM000681.1:g.15349647G>A	GRCh37
NC_000019.8:g.15210647G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679869.1:c.3927C>T MANE Select	ENSP00000506350.1:p.Thr1309=
ENST00000263377.6:c.3927C>T	ENSP00000263377.1:p.Thr1309=
NM_058243.2:c.3927C>T	NP_490597.1:p.Thr1309=
XM_011527854.1:c.3927C>T	XP_011526156.1:p.Thr1309=
XM_011527854.2:c.3927C>T	XP_011526156.1:p.Thr1309=
NM_001379291.1:c.3927C>T MANE Select	NP_001366220.1:p.Thr1309=
NM_058243.3:c.3927C>T	NP_490597.1:p.Thr1309=