Canonical Allele Identifier: CA2634409718

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099503-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099503T>C , CM000678.2:g.78099503T>C	GRCh38
NC_000016.9:g.78133400T>C , CM000678.1:g.78133400T>C	GRCh37
NC_000016.8:g.76690901T>C	NCBI36
NG_011698.1:g.4850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-276T>C	ENSP00000485925.2:n.-276T>C
ENST00000682609.1:n.52T>C
ENST00000683286.1:n.52T>C
ENST00000683929.1:c.-276T>C	ENSP00000507689.1:n.-276T>C
ENST00000684070.1:n.54T>C
ENST00000684381.1:n.52T>C
ENST00000684452.1:n.52T>C
ENST00000684632.1:n.104T>C
ENST00000566780.5:c.-276T>C	ENSP00000457230.1:n.-276T>C
ENST00000627394.2:c.-276T>C	ENSP00000485925.1:n.-276T>C
NM_001291997.1:c.-550T>C	NP_001278926.1:n.-550T>C
NM_016373.3:c.-276T>C	NP_057457.1:n.-276T>C
NM_130791.3:c.-276T>C	NP_570607.1:n.-276T>C
NR_120435.1:n.91T>C
NR_120436.1:n.91T>C