Canonical Allele Identifier: CA337722125
Gene: DDX3Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2032590

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12907702T>G , CM000686.2:g.12907702T>G GRCh38
NC_000024.9:g.15019613T>G , CM000686.1:g.15019613T>G GRCh37
NC_000024.8:g.13529007T>G NCBI36
NG_012831.1:g.8595T>G

Transcript Alleles

HGVS Amino-acid change
NM_001122665.2:c.103+108T>G VV NP_001116137.1:p.=
NM_001302552.1:c.94+108T>G VV NP_001289481.1:p.=
NM_004660.4:c.103+108T>G VV NP_004651.2:p.=
XM_006724878.1:c.103+108T>G XP_006724941.1:p.=
XM_011531471.1:c.103+108T>G XP_011529773.1:p.=
NM_001122665.3:c.103+108T>G VV NP_001116137.1:p.=
NM_001302552.2:c.94+108T>G VV NP_001289481.1:p.=
NM_001324195.1:c.103+108T>G VV NP_001311124.1:p.=
NR_136716.1:n.254+108T>G
NR_136717.1:n.254+108T>G
NR_136718.1:n.254+108T>G
NR_136719.1:n.254+108T>G
NR_136720.1:n.254+108T>G
NR_136721.1:n.182+108T>G
NR_136722.1:n.169+108T>G
NR_136723.1:n.169+108T>G
NR_136724.1:n.169+108T>G
XR_001756014.2:n.207+108T>G
NM_004660.5:c.103+108T>G VV MANE Preferred NP_004651.2:p.=
ENST00000336079.7:c.103+108T>G ENSP00000336725.3:p.=
ENST00000360160.8:c.103+108T>G ENSP00000353284.4:p.=
ENST00000440554.1:c.94+108T>G ENSP00000400377.1:p.=
ENST00000454054.5:c.103+108T>G ENSP00000398953.1:p.=
ENST00000493363.1:n.191+108T>G