Canonical Allele Identifier: CA284501424

Gene: WWOX

Linked Data

• dbSNP Id: rs907253126
• gnomAD v2: 16-78133314-T-C
• gnomAD v3: 16-78099417-T-C
• gnomAD v4: 16-78099417-T-C
• MyVariant Identifiers: chr16:g.78133314T>C (hg19) ; chr16:g.78099417T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099417T>C , CM000678.2:g.78099417T>C	GRCh38
NC_000016.9:g.78133314T>C , CM000678.1:g.78133314T>C	GRCh37
NC_000016.8:g.76690815T>C	NCBI36
NG_011698.1:g.4764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-362T>C	ENSP00000485925.2:n.-362T>C
ENST00000683929.1:c.-362T>C	ENSP00000507689.1:n.-362T>C
ENST00000684632.1:n.18T>C
ENST00000566780.5:c.-362T>C	ENSP00000457230.1:n.-362T>C
NM_001291997.1:c.-636T>C	NP_001278926.1:n.-636T>C
NM_016373.3:c.-362T>C	NP_057457.1:n.-362T>C
NM_130791.3:c.-362T>C	NP_570607.1:n.-362T>C
NR_120435.1:n.5T>C
NR_120436.1:n.5T>C