Canonical Allele Identifier: CA2694175639

Gene: BRWD3

Linked Data

• gnomAD v4: X-80745555-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745555A>C , CM000685.2:g.80745555A>C	GRCh38
NC_000023.10:g.80001054A>C , CM000685.1:g.80001054A>C	GRCh37
NC_000023.9:g.79887710A>C	NCBI36
NG_021349.1:g.69180T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.591+14T>G MANE Select	ENSP00000362372.4:n.591+14T>G
ENST00000373275.4:c.591+14T>G	ENSP00000362372.4:n.591+14T>G
ENST00000478415.1:n.803+14T>G
NM_153252.4:c.591+14T>G	NP_694984.4:n.591+14T>G
XM_005262113.2:c.591+14T>G	XP_005262170.1:n.591+14T>G
XM_011530903.1:c.78+14T>G	XP_011529205.1:n.78+14T>G
XM_011530904.1:c.-746+14T>G	XP_011529206.1:n.-746+14T>G
XR_430519.2:n.854+14T>G
XM_005262113.3:c.591+14T>G	XP_005262170.1:n.591+14T>G
XM_017029384.1:c.-746+14T>G	XP_016884873.1:n.-746+14T>G
XM_017029385.2:c.591+14T>G	XP_016884874.1:n.591+14T>G
XR_430519.3:n.856+14T>G
NM_153252.5:c.591+14T>G MANE Select	NP_694984.5:n.591+14T>G