Canonical Allele Identifier: CA2634409728

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099515-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099515G>T , CM000678.2:g.78099515G>T	GRCh38
NC_000016.9:g.78133412G>T , CM000678.1:g.78133412G>T	GRCh37
NC_000016.8:g.76690913G>T	NCBI36
NG_011698.1:g.4862G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-264G>T	ENSP00000485925.2:n.-264G>T
ENST00000682609.1:n.64G>T
ENST00000683286.1:n.64G>T
ENST00000683929.1:c.-264G>T	ENSP00000507689.1:n.-264G>T
ENST00000684070.1:n.66G>T
ENST00000684381.1:n.64G>T
ENST00000684452.1:n.64G>T
ENST00000684632.1:n.116G>T
ENST00000566780.5:c.-264G>T	ENSP00000457230.1:n.-264G>T
ENST00000627394.2:c.-264G>T	ENSP00000485925.1:n.-264G>T
NM_001291997.1:c.-538G>T	NP_001278926.1:n.-538G>T
NM_016373.3:c.-264G>T	NP_057457.1:n.-264G>T
NM_130791.3:c.-264G>T	NP_570607.1:n.-264G>T
NR_120435.1:n.103G>T
NR_120436.1:n.103G>T