Canonical Allele Identifier: CA2694175667

Gene: BRWD3

Linked Data

• gnomAD v4: X-80745796-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745796A>T , CM000685.2:g.80745796A>T	GRCh38
NC_000023.10:g.80001295A>T , CM000685.1:g.80001295A>T	GRCh37
NC_000023.9:g.79887951A>T	NCBI36
NG_021349.1:g.68939T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-67T>A MANE Select	ENSP00000362372.4:n.431-67T>A
ENST00000373275.4:c.431-67T>A	ENSP00000362372.4:n.431-67T>A
ENST00000478415.1:n.643-67T>A
NM_153252.4:c.431-67T>A	NP_694984.4:n.431-67T>A
XM_005262113.2:c.431-67T>A	XP_005262170.1:n.431-67T>A
XM_011530903.1:c.-83-67T>A	XP_011529205.1:n.-83-67T>A
XM_011530904.1:c.-906-67T>A	XP_011529206.1:n.-906-67T>A
XR_430519.2:n.694-67T>A
XM_005262113.3:c.431-67T>A	XP_005262170.1:n.431-67T>A
XM_017029384.1:c.-906-67T>A	XP_016884873.1:n.-906-67T>A
XM_017029385.2:c.431-67T>A	XP_016884874.1:n.431-67T>A
XR_430519.3:n.696-67T>A
NM_153252.5:c.431-67T>A MANE Select	NP_694984.5:n.431-67T>A