Canonical Allele Identifier: CA413607390

Gene: BRWD3

Linked Data

• dbSNP Id: rs1602386544
• MyVariant Identifiers: chrX:g.80001100C>T (hg19) ; chrX:g.80745601C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745601C>T , CM000685.2:g.80745601C>T	GRCh38
NC_000023.10:g.80001100C>T , CM000685.1:g.80001100C>T	GRCh37
NC_000023.9:g.79887756C>T	NCBI36
NG_021349.1:g.69134G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373275.5:c.559G>A MANE Select	ENSP00000362372.4:p.Ala187Thr
ENST00000373275.4:c.559G>A	ENSP00000362372.4:p.Ala187Thr
ENST00000478415.1:n.771G>A
NM_153252.4:c.559G>A	NP_694984.4:p.Ala187Thr
XM_005262113.2:c.559G>A	XP_005262170.1:p.Ala187Thr
XM_011530903.1:c.46G>A	XP_011529205.1:p.Ala16Thr
XM_011530904.1:c.-778G>A	XP_011529206.1:n.-778G>A
XR_430519.2:n.822G>A
XM_005262113.3:c.559G>A	XP_005262170.1:p.Ala187Thr
XM_017029384.1:c.-778G>A	XP_016884873.1:n.-778G>A
XM_017029385.2:c.559G>A	XP_016884874.1:p.Ala187Thr
XR_430519.3:n.824G>A
NM_153252.5:c.559G>A MANE Select	NP_694984.5:p.Ala187Thr