Canonical Allele Identifier: CA10573788
Gene: DDX3Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2032649

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12917580T>G , CM000686.2:g.12917580T>G GRCh38
NC_000024.9:g.15029492T>G , CM000686.1:g.15029492T>G GRCh37
NC_000024.8:g.13538886T>G NCBI36
NG_012831.1:g.18474T>G

Transcript Alleles

HGVS Amino-acid change
NM_001122665.2:c.1903+38T>G VV NP_001116137.1:p.=
NM_001302552.1:c.1894+38T>G VV NP_001289481.1:p.=
NM_004660.4:c.1903+38T>G VV NP_004651.2:p.=
XM_006724878.1:c.1834+38T>G XP_006724941.1:p.=
NM_001122665.3:c.1903+38T>G VV NP_001116137.1:p.=
NM_001302552.2:c.1894+38T>G VV NP_001289481.1:p.=
NM_001324195.1:c.1834+38T>G VV NP_001311124.1:p.=
NR_136716.1:n.2372+38T>G
NR_136717.1:n.2134+38T>G
NR_136718.1:n.2452+38T>G
NR_136719.1:n.2242+38T>G
NR_136720.1:n.2303+38T>G
NR_136721.1:n.1965+38T>G
NR_136722.1:n.2049+38T>G
NR_136723.1:n.2367+38T>G
NR_136724.1:n.2287+38T>G
XR_001756014.2:n.2067+38T>G
NM_004660.5:c.1903+38T>G VV MANE Preferred NP_004651.2:p.=
ENST00000336079.7:c.1903+38T>G ENSP00000336725.3:p.=
ENST00000360160.8:c.1903+38T>G ENSP00000353284.4:p.=