Canonical Allele Identifier: CA878678249

Gene: BRWD3

Linked Data

• dbSNP Id: rs1439998406
• gnomAD v3: X-80745749-A-C
• gnomAD v4: X-80745749-A-C
• MyVariant Identifiers: chrX:g.80001248A>C (hg19) ; chrX:g.80745749A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745749A>C , CM000685.2:g.80745749A>C	GRCh38
NC_000023.10:g.80001248A>C , CM000685.1:g.80001248A>C	GRCh37
NC_000023.9:g.79887904A>C	NCBI36
NG_021349.1:g.68986T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-20T>G MANE Select	ENSP00000362372.4:n.431-20T>G
ENST00000373275.4:c.431-20T>G	ENSP00000362372.4:n.431-20T>G
ENST00000478415.1:n.643-20T>G
NM_153252.4:c.431-20T>G	NP_694984.4:n.431-20T>G
XM_005262113.2:c.431-20T>G	XP_005262170.1:n.431-20T>G
XM_011530903.1:c.-83-20T>G	XP_011529205.1:n.-83-20T>G
XM_011530904.1:c.-906-20T>G	XP_011529206.1:n.-906-20T>G
XR_430519.2:n.694-20T>G
XM_005262113.3:c.431-20T>G	XP_005262170.1:n.431-20T>G
XM_017029384.1:c.-906-20T>G	XP_016884873.1:n.-906-20T>G
XM_017029385.2:c.431-20T>G	XP_016884874.1:n.431-20T>G
XR_430519.3:n.696-20T>G
NM_153252.5:c.431-20T>G MANE Select	NP_694984.5:n.431-20T>G