Canonical Allele Identifier: CA9264657
Gene: BRD4 HGNC NCBI
ClinVar RCV:
RCV001541001
ClinVar Variation:
1183214
dbSNP:
60057301
gnomAD v2:
19:15350367 C / T
gnomAD v3:
19:15239556 C / T
gnomAD v4:
chr19-15239556-C-T
Joint Max Group AF 0.05188345 (AFR)
Genomes Max Group AF 0.05161159 (AFR)
Exomes Max Group AF 0.05094363 (AFR)
MyVariant.info:
GRCh38 chr19:g.15239556C>T
GRCh37 chr19:g.15350367C>T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15239556C>T , CM000681.2:g.15239556C>T GRCh38
NC_000019.9:g.15350367C>T , CM000681.1:g.15350367C>T GRCh37
NC_000019.8:g.15211367C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679869.1:c.3446-34G>A MANE Select ENSP00000506350.1:n.3446-34G>A
ENST00000263377.6:c.3446-34G>A ENSP00000263377.1:n.3446-34G>A
NM_058243.2:c.3446-34G>A NP_490597.1:n.3446-34G>A
XM_011527854.1:c.3446-34G>A XP_011526156.1:n.3446-34G>A
XM_011527854.2:c.3446-34G>A XP_011526156.1:n.3446-34G>A
NM_001379291.1:c.3446-34G>A MANE Select NP_001366220.1:n.3446-34G>A
NM_058243.3:c.3446-34G>A NP_490597.1:n.3446-34G>A
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