Canonical Allele Identifier: CA517056372

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001211T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745712T>G , CM000685.2:g.80745712T>G	GRCh38
NC_000023.10:g.80001211T>G , CM000685.1:g.80001211T>G	GRCh37
NC_000023.9:g.79887867T>G	NCBI36
NG_021349.1:g.69023A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.448A>C MANE Select	ENSP00000362372.4:p.Arg150=
ENST00000373275.4:c.448A>C	ENSP00000362372.4:p.Arg150=
ENST00000478415.1:n.660A>C
NM_153252.4:c.448A>C	NP_694984.4:p.Arg150=
XM_005262113.2:c.448A>C	XP_005262170.1:p.Arg150=
XM_011530903.1:c.-66A>C	XP_011529205.1:n.-66A>C
XM_011530904.1:c.-889A>C	XP_011529206.1:n.-889A>C
XR_430519.2:n.711A>C
XM_005262113.3:c.448A>C	XP_005262170.1:p.Arg150=
XM_017029384.1:c.-889A>C	XP_016884873.1:n.-889A>C
XM_017029385.2:c.448A>C	XP_016884874.1:p.Arg150=
XR_430519.3:n.713A>C
NM_153252.5:c.448A>C MANE Select	NP_694984.5:p.Arg150=