Canonical Allele Identifier: CA331097292

Gene: BRWD3

Linked Data

• dbSNP Id: rs2203205
• gnomAD v2: X-80008883-C-T
• gnomAD v3: X-80753384-C-T
• gnomAD v4: X-80753384-C-T
• MyVariant Identifiers: chrX:g.80008883C>T (hg19) ; chrX:g.80753384C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80753384C>T , CM000685.2:g.80753384C>T	GRCh38
NC_000023.10:g.80008883C>T , CM000685.1:g.80008883C>T	GRCh37
NC_000023.9:g.79895539C>T	NCBI36
NG_021349.1:g.61351G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373275.5:c.431-7655G>A MANE Select	ENSP00000362372.4:n.431-7655G>A
ENST00000373275.4:c.431-7655G>A	ENSP00000362372.4:n.431-7655G>A
ENST00000478415.1:n.643-7655G>A
NM_153252.4:c.431-7655G>A	NP_694984.4:n.431-7655G>A
XM_005262113.2:c.431-7655G>A	XP_005262170.1:n.431-7655G>A
XM_011530903.1:c.-83-7655G>A	XP_011529205.1:n.-83-7655G>A
XM_011530904.1:c.-906-7655G>A	XP_011529206.1:n.-906-7655G>A
XR_430519.2:n.694-7655G>A
XM_005262113.3:c.431-7655G>A	XP_005262170.1:n.431-7655G>A
XM_017029384.1:c.-906-7655G>A	XP_016884873.1:n.-906-7655G>A
XM_017029385.2:c.431-7655G>A	XP_016884874.1:n.431-7655G>A
XR_430519.3:n.696-7655G>A
NM_153252.5:c.431-7655G>A MANE Select	NP_694984.5:n.431-7655G>A