Canonical Allele Identifier: CA413607667

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001206T>A (hg19) ; chrX:g.80745707T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745707T>A , CM000685.2:g.80745707T>A	GRCh38
NC_000023.10:g.80001206T>A , CM000685.1:g.80001206T>A	GRCh37
NC_000023.9:g.79887862T>A	NCBI36
NG_021349.1:g.69028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.453A>T MANE Select	ENSP00000362372.4:p.Gln151His
ENST00000373275.4:c.453A>T	ENSP00000362372.4:p.Gln151His
ENST00000478415.1:n.665A>T
NM_153252.4:c.453A>T	NP_694984.4:p.Gln151His
XM_005262113.2:c.453A>T	XP_005262170.1:p.Gln151His
XM_011530903.1:c.-61A>T	XP_011529205.1:n.-61A>T
XM_011530904.1:c.-884A>T	XP_011529206.1:n.-884A>T
XR_430519.2:n.716A>T
XM_005262113.3:c.453A>T	XP_005262170.1:p.Gln151His
XM_017029384.1:c.-884A>T	XP_016884873.1:n.-884A>T
XM_017029385.2:c.453A>T	XP_016884874.1:p.Gln151His
XR_430519.3:n.718A>T
NM_153252.5:c.453A>T MANE Select	NP_694984.5:p.Gln151His