Canonical Allele Identifier: CA2440263031

Gene: BRWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745681T= , CM000685.2:g.80745681T=	GRCh38
NC_000023.10:g.80001180T= , CM000685.1:g.80001180T=	GRCh37
NC_000023.9:g.79887836T=	NCBI36
NG_021349.1:g.69054A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.479A= MANE Select	ENSP00000362372.4:p.His160=
ENST00000373275.4:c.479A=	ENSP00000362372.4:p.His160=
ENST00000478415.1:n.691A=
NM_153252.4:c.479A=	NP_694984.4:p.His160=
XM_005262113.2:c.479A=	XP_005262170.1:p.His160=
XM_011530903.1:c.-35A=	XP_011529205.1:n.-35A=
XM_011530904.1:c.-858A=	XP_011529206.1:n.-858A=
XR_430519.2:n.742A=
XM_005262113.3:c.479A=	XP_005262170.1:p.His160=
XM_017029384.1:c.-858A=	XP_016884873.1:n.-858A=
XM_017029385.2:c.479A=	XP_016884874.1:p.His160=
XR_430519.3:n.744A=
NM_153252.5:c.479A= MANE Select	NP_694984.5:p.His160=