Canonical Allele Identifier: CA413607719

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001230T>C (hg19) ; chrX:g.80745731T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745731T>C , CM000685.2:g.80745731T>C	GRCh38
NC_000023.10:g.80001230T>C , CM000685.1:g.80001230T>C	GRCh37
NC_000023.9:g.79887886T>C	NCBI36
NG_021349.1:g.69004A>G

Transcript Alleles

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