Canonical Allele Identifier: CA10654385

Gene: BRWD3

Linked Data

• ClinVar Variation Id: 368680
• ClinVar RCV Id: RCV000341194
• dbSNP Id: rs2063579
• gnomAD v2: X-79925246-A-G
• gnomAD v3: X-80669747-A-G
• gnomAD v4: X-80669747-A-G
• MyVariant Identifiers: chrX:g.79925246A>G (hg19) ; chrX:g.80669747A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80669747A>G , CM000685.2:g.80669747A>G	GRCh38
NC_000023.10:g.79925246A>G , CM000685.1:g.79925246A>G	GRCh37
NC_000023.9:g.79811902A>G	NCBI36
NG_021349.1:g.144988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.*6862T>C MANE Select	ENSP00000362372.4:n.*6862T>C
NM_153252.4:c.*6862T>C	NP_694984.4:n.*6862T>C
XM_005262113.2:c.*6862T>C	XP_005262170.1:n.*6862T>C
XM_011530903.1:c.*6862T>C	XP_011529205.1:n.*6862T>C
XM_011530904.1:c.*6862T>C	XP_011529206.1:n.*6862T>C
XM_005262113.3:c.*6862T>C	XP_005262170.1:n.*6862T>C
NM_153252.5:c.*6862T>C MANE Select	NP_694984.5:n.*6862T>C