Canonical Allele Identifier: CA2694175641

Gene: BRWD3

Linked Data

• gnomAD v4: X-80745566-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745566C>A , CM000685.2:g.80745566C>A	GRCh38
NC_000023.10:g.80001065C>A , CM000685.1:g.80001065C>A	GRCh37
NC_000023.9:g.79887721C>A	NCBI36
NG_021349.1:g.69169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.591+3G>T MANE Select	ENSP00000362372.4:n.591+3G>T
ENST00000373275.4:c.591+3G>T	ENSP00000362372.4:n.591+3G>T
ENST00000478415.1:n.803+3G>T
NM_153252.4:c.591+3G>T	NP_694984.4:n.591+3G>T
XM_005262113.2:c.591+3G>T	XP_005262170.1:n.591+3G>T
XM_011530903.1:c.78+3G>T	XP_011529205.1:n.78+3G>T
XM_011530904.1:c.-746+3G>T	XP_011529206.1:n.-746+3G>T
XR_430519.2:n.854+3G>T
XM_005262113.3:c.591+3G>T	XP_005262170.1:n.591+3G>T
XM_017029384.1:c.-746+3G>T	XP_016884873.1:n.-746+3G>T
XM_017029385.2:c.591+3G>T	XP_016884874.1:n.591+3G>T
XR_430519.3:n.856+3G>T
NM_153252.5:c.591+3G>T MANE Select	NP_694984.5:n.591+3G>T