Canonical Allele Identifier: CA623696476

Gene: WWOX

Linked Data

• dbSNP Id: rs1486628286
• gnomAD v2: 16-78569866-A-T
• gnomAD v3: 16-78535969-A-T
• gnomAD v4: 16-78535969-A-T
• MyVariant Identifiers: chr16:g.78569866A>T (hg19) ; chr16:g.78535969A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78535969A>T , CM000678.2:g.78535969A>T	GRCh38
NC_000016.9:g.78569866A>T , CM000678.1:g.78569866A>T	GRCh37
NC_000016.8:g.77127367A>T	NCBI36
NG_011698.1:g.441316A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1152+127A>T	ENSP00000485925.2:n.1152+127A>T
ENST00000683929.1:c.1056+103217A>T	ENSP00000507689.1:n.1056+103217A>T
ENST00000684632.1:n.1436-99878A>T
ENST00000566780.6:c.1056+103217A>T MANE Select	ENSP00000457230.1:n.1056+103217A>T
ENST00000402655.6:c.409+420815A>T	ENSP00000384238.2:n.409+420815A>T
ENST00000406884.6:c.516+371680A>T	ENSP00000384495.2:n.516+371680A>T
ENST00000408984.7:c.1056+103217A>T	ENSP00000386161.3:n.1056+103217A>T
ENST00000539474.6:c.410-220971A>T	ENSP00000445210.2:n.410-220971A>T
ENST00000566780.5:c.1056+103217A>T	ENSP00000457230.1:n.1056+103217A>T
ENST00000569332.5:c.*853+103217A>T	ENSP00000454788.1:n.*853+103217A>T
NM_001291997.1:c.717+103217A>T	NP_001278926.1:n.717+103217A>T
NM_016373.3:c.1056+103217A>T	NP_057457.1:n.1056+103217A>T
XM_011523100.1:c.1152+127A>T	XP_011521402.1:n.1152+127A>T
XM_011523101.1:c.1057-38090A>T	XP_011521403.1:n.1057-38090A>T
XM_011523103.1:c.1056+103217A>T	XP_011521405.1:n.1056+103217A>T
XM_011523101.3:c.1057-38090A>T	XP_011521403.1:n.1057-38090A>T
XM_011523103.3:c.1056+103217A>T	XP_011521405.1:n.1056+103217A>T
XM_017023279.1:c.142+127A>T	XP_016878768.1:n.142+127A>T
NM_016373.4:c.1056+103217A>T MANE Select	NP_057457.1:n.1056+103217A>T
NM_001291997.2:c.717+103217A>T	NP_001278926.1:n.717+103217A>T