Canonical Allele Identifier: CA1134661674

Gene: BRWD3

Linked Data

• dbSNP Id: rs2073585739
• gnomAD v3: X-80745875-C-G
• gnomAD v4: X-80745875-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745875C>G , CM000685.2:g.80745875C>G	GRCh38
NC_000023.10:g.80001374C>G , CM000685.1:g.80001374C>G	GRCh37
NC_000023.9:g.79888030C>G	NCBI36
NG_021349.1:g.68860G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-146G>C MANE Select	ENSP00000362372.4:n.431-146G>C
ENST00000373275.4:c.431-146G>C	ENSP00000362372.4:n.431-146G>C
ENST00000478415.1:n.643-146G>C
NM_153252.4:c.431-146G>C	NP_694984.4:n.431-146G>C
XM_005262113.2:c.431-146G>C	XP_005262170.1:n.431-146G>C
XM_011530903.1:c.-83-146G>C	XP_011529205.1:n.-83-146G>C
XM_011530904.1:c.-906-146G>C	XP_011529206.1:n.-906-146G>C
XR_430519.2:n.694-146G>C
XM_005262113.3:c.431-146G>C	XP_005262170.1:n.431-146G>C
XM_017029384.1:c.-906-146G>C	XP_016884873.1:n.-906-146G>C
XM_017029385.2:c.431-146G>C	XP_016884874.1:n.431-146G>C
XR_430519.3:n.696-146G>C
NM_153252.5:c.431-146G>C MANE Select	NP_694984.5:n.431-146G>C