Canonical Allele Identifier: CA623600957

Gene: WWOX

Linked Data

• dbSNP Id: rs1464185039
• gnomAD v2: 16-78133519-C-T
• gnomAD v3: 16-78099622-C-T
• gnomAD v4: 16-78099622-C-T
• MyVariant Identifiers: chr16:g.78133519C>T (hg19) ; chr16:g.78099622C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099622C>T , CM000678.2:g.78099622C>T	GRCh38
NC_000016.9:g.78133519C>T , CM000678.1:g.78133519C>T	GRCh37
NC_000016.8:g.76691020C>T	NCBI36
NG_011698.1:g.4969C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-157C>T	ENSP00000485925.2:n.-157C>T
ENST00000682609.1:n.171C>T
ENST00000683286.1:n.171C>T
ENST00000683929.1:c.-157C>T	ENSP00000507689.1:n.-157C>T
ENST00000684070.1:n.173C>T
ENST00000684381.1:n.171C>T
ENST00000684452.1:n.171C>T
ENST00000684632.1:n.223C>T
ENST00000566780.5:c.-157C>T	ENSP00000457230.1:n.-157C>T
ENST00000627394.2:c.-157C>T	ENSP00000485925.1:n.-157C>T
NM_001291997.1:c.-431C>T	NP_001278926.1:n.-431C>T
NM_016373.3:c.-157C>T	NP_057457.1:n.-157C>T
NM_130791.3:c.-157C>T	NP_570607.1:n.-157C>T
NR_120435.1:n.210C>T
NR_120436.1:n.210C>T