Canonical Allele Identifier: CA517056313

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001136T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745637T>G , CM000685.2:g.80745637T>G	GRCh38
NC_000023.10:g.80001136T>G , CM000685.1:g.80001136T>G	GRCh37
NC_000023.9:g.79887792T>G	NCBI36
NG_021349.1:g.69098A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.523A>C MANE Select	ENSP00000362372.4:p.Arg175=
ENST00000373275.4:c.523A>C	ENSP00000362372.4:p.Arg175=
ENST00000478415.1:n.735A>C
NM_153252.4:c.523A>C	NP_694984.4:p.Arg175=
XM_005262113.2:c.523A>C	XP_005262170.1:p.Arg175=
XM_011530903.1:c.10A>C	XP_011529205.1:p.Arg4=
XM_011530904.1:c.-814A>C	XP_011529206.1:n.-814A>C
XR_430519.2:n.786A>C
XM_005262113.3:c.523A>C	XP_005262170.1:p.Arg175=
XM_017029384.1:c.-814A>C	XP_016884873.1:n.-814A>C
XM_017029385.2:c.523A>C	XP_016884874.1:p.Arg175=
XR_430519.3:n.788A>C
NM_153252.5:c.523A>C MANE Select	NP_694984.5:p.Arg175=