Canonical Allele Identifier: CA2694175673

Gene: BRWD3

Linked Data

• gnomAD v4: X-80745815-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745815C>G , CM000685.2:g.80745815C>G	GRCh38
NC_000023.10:g.80001314C>G , CM000685.1:g.80001314C>G	GRCh37
NC_000023.9:g.79887970C>G	NCBI36
NG_021349.1:g.68920G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-86G>C MANE Select	ENSP00000362372.4:n.431-86G>C
ENST00000373275.4:c.431-86G>C	ENSP00000362372.4:n.431-86G>C
ENST00000478415.1:n.643-86G>C
NM_153252.4:c.431-86G>C	NP_694984.4:n.431-86G>C
XM_005262113.2:c.431-86G>C	XP_005262170.1:n.431-86G>C
XM_011530903.1:c.-83-86G>C	XP_011529205.1:n.-83-86G>C
XM_011530904.1:c.-906-86G>C	XP_011529206.1:n.-906-86G>C
XR_430519.2:n.694-86G>C
XM_005262113.3:c.431-86G>C	XP_005262170.1:n.431-86G>C
XM_017029384.1:c.-906-86G>C	XP_016884873.1:n.-906-86G>C
XM_017029385.2:c.431-86G>C	XP_016884874.1:n.431-86G>C
XR_430519.3:n.696-86G>C
NM_153252.5:c.431-86G>C MANE Select	NP_694984.5:n.431-86G>C