Canonical Allele Identifier: CA337722265
Gene: DDX3Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2032624
MyVariant Identifiers: chrY:g.12914512C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914512C>A , CM000686.2:g.12914512C>A GRCh38
NC_000024.9:g.15026424C>A , CM000686.1:g.15026424C>A GRCh37
NC_000024.8:g.13535818C>A NCBI36
NG_012831.1:g.15406C>A

Transcript Alleles

HGVS Amino-acid change
NM_001122665.2:c.674-52C>A VV NP_001116137.1:p.=
NM_001302552.1:c.665-52C>A VV NP_001289481.1:p.=
NM_004660.4:c.674-52C>A VV NP_004651.2:p.=
XM_006724878.1:c.674-52C>A XP_006724941.1:p.=
XM_011531471.1:c.674-52C>A XP_011529773.1:p.=
NM_001122665.3:c.674-52C>A VV NP_001116137.1:p.=
NM_001302552.2:c.665-52C>A VV NP_001289481.1:p.=
NM_001324195.1:c.674-52C>A VV NP_001311124.1:p.=
NR_136716.1:n.825-52C>A
NR_136717.1:n.905-52C>A
NR_136718.1:n.905-52C>A
NR_136719.1:n.695-52C>A
NR_136720.1:n.825-52C>A
NR_136721.1:n.753-52C>A
NR_136722.1:n.820-52C>A
NR_136723.1:n.820-52C>A
NR_136724.1:n.740-52C>A
XR_001756014.2:n.778-52C>A
NM_004660.5:c.674-52C>A VV MANE Preferred NP_004651.2:p.=
ENST00000336079.7:c.674-52C>A ENSP00000336725.3:p.=
ENST00000360160.8:c.674-52C>A ENSP00000353284.4:p.=
ENST00000440554.1:c.665-52C>A ENSP00000400377.1:p.=
ENST00000463199.1:n.192-52C>A
ENST00000472510.5:n.237-52C>A