Canonical Allele Identifier: CA284501821

Gene: WWOX

Linked Data

• dbSNP Id: rs548639061
• gnomAD v4: 16-78099564-C-T
• MyVariant Identifiers: chr16:g.78133461C>T (hg19) ; chr16:g.78099564C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099564C>T , CM000678.2:g.78099564C>T	GRCh38
NC_000016.9:g.78133461C>T , CM000678.1:g.78133461C>T	GRCh37
NC_000016.8:g.76690962C>T	NCBI36
NG_011698.1:g.4911C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-215C>T	ENSP00000485925.2:n.-215C>T
ENST00000682609.1:n.113C>T
ENST00000683286.1:n.113C>T
ENST00000683929.1:c.-215C>T	ENSP00000507689.1:n.-215C>T
ENST00000684070.1:n.115C>T
ENST00000684381.1:n.113C>T
ENST00000684452.1:n.113C>T
ENST00000684632.1:n.165C>T
ENST00000566780.5:c.-215C>T	ENSP00000457230.1:n.-215C>T
ENST00000627394.2:c.-215C>T	ENSP00000485925.1:n.-215C>T
NM_001291997.1:c.-489C>T	NP_001278926.1:n.-489C>T
NM_016373.3:c.-215C>T	NP_057457.1:n.-215C>T
NM_130791.3:c.-215C>T	NP_570607.1:n.-215C>T
NR_120435.1:n.152C>T
NR_120436.1:n.152C>T