Canonical Allele Identifier: CA10462354

Gene: BRWD3

Linked Data

• dbSNP Id: rs373686108
• ExAC: X:80001202 T / A
• gnomAD v2: X-80001202-T-A
• gnomAD v4: X-80745703-T-A
• MyVariant Identifiers: chrX:g.80001202T>A (hg19) ; chrX:g.80745703T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745703T>A , CM000685.2:g.80745703T>A	GRCh38
NC_000023.10:g.80001202T>A , CM000685.1:g.80001202T>A	GRCh37
NC_000023.9:g.79887858T>A	NCBI36
NG_021349.1:g.69032A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.457A>T MANE Select	ENSP00000362372.4:p.Thr153Ser
ENST00000373275.4:c.457A>T	ENSP00000362372.4:p.Thr153Ser
ENST00000478415.1:n.669A>T
NM_153252.4:c.457A>T	NP_694984.4:p.Thr153Ser
XM_005262113.2:c.457A>T	XP_005262170.1:p.Thr153Ser
XM_011530903.1:c.-57A>T	XP_011529205.1:n.-57A>T
XM_011530904.1:c.-880A>T	XP_011529206.1:n.-880A>T
XR_430519.2:n.720A>T
XM_005262113.3:c.457A>T	XP_005262170.1:p.Thr153Ser
XM_017029384.1:c.-880A>T	XP_016884873.1:n.-880A>T
XM_017029385.2:c.457A>T	XP_016884874.1:p.Thr153Ser
XR_430519.3:n.722A>T
NM_153252.5:c.457A>T MANE Select	NP_694984.5:p.Thr153Ser