Canonical Allele Identifier: CA623600946

Gene: WWOX

Linked Data

• dbSNP Id: rs1244578211
• gnomAD v2: 16-78133424-G-T
• gnomAD v3: 16-78099527-G-T
• gnomAD v4: 16-78099527-G-T
• MyVariant Identifiers: chr16:g.78133424G>T (hg19) ; chr16:g.78099527G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099527G>T , CM000678.2:g.78099527G>T	GRCh38
NC_000016.9:g.78133424G>T , CM000678.1:g.78133424G>T	GRCh37
NC_000016.8:g.76690925G>T	NCBI36
NG_011698.1:g.4874G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-252G>T	ENSP00000485925.2:n.-252G>T
ENST00000682609.1:n.76G>T
ENST00000683286.1:n.76G>T
ENST00000683929.1:c.-252G>T	ENSP00000507689.1:n.-252G>T
ENST00000684070.1:n.78G>T
ENST00000684381.1:n.76G>T
ENST00000684452.1:n.76G>T
ENST00000684632.1:n.128G>T
ENST00000566780.5:c.-252G>T	ENSP00000457230.1:n.-252G>T
ENST00000627394.2:c.-252G>T	ENSP00000485925.1:n.-252G>T
NM_001291997.1:c.-526G>T	NP_001278926.1:n.-526G>T
NM_016373.3:c.-252G>T	NP_057457.1:n.-252G>T
NM_130791.3:c.-252G>T	NP_570607.1:n.-252G>T
NR_120435.1:n.115G>T
NR_120436.1:n.115G>T