Canonical Allele Identifier: CA2440263058

Gene: BRWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745751C= , CM000685.2:g.80745751C=	GRCh38
NC_000023.10:g.80001250C= , CM000685.1:g.80001250C=	GRCh37
NC_000023.9:g.79887906C=	NCBI36
NG_021349.1:g.68984G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-22G= MANE Select	ENSP00000362372.4:n.431-22G=
ENST00000373275.4:c.431-22G=	ENSP00000362372.4:n.431-22G=
ENST00000478415.1:n.643-22G=
NM_153252.4:c.431-22G=	NP_694984.4:n.431-22G=
XM_005262113.2:c.431-22G=	XP_005262170.1:n.431-22G=
XM_011530903.1:c.-83-22G=	XP_011529205.1:n.-83-22G=
XM_011530904.1:c.-906-22G=	XP_011529206.1:n.-906-22G=
XR_430519.2:n.694-22G=
XM_005262113.3:c.431-22G=	XP_005262170.1:n.431-22G=
XM_017029384.1:c.-906-22G=	XP_016884873.1:n.-906-22G=
XM_017029385.2:c.431-22G=	XP_016884874.1:n.431-22G=
XR_430519.3:n.696-22G=
NM_153252.5:c.431-22G= MANE Select	NP_694984.5:n.431-22G=