Canonical Allele Identifier: CA10573655
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs2032610
ExAC: Y:15025598 T / C
gnomAD v2: Y-15025598-T-C
gnomAD v3: Y-12913686-T-C
gnomAD v4: Y-12913686-T-C
MyVariant Identifiers: chrY:g.15025598T>C (hg19) chrY:g.12913686T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12913686T>C , CM000686.2:g.12913686T>C GRCh38
NC_000024.9:g.15025598T>C , CM000686.1:g.15025598T>C GRCh37
NC_000024.8:g.13534992T>C NCBI36
NG_012831.1:g.14580T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.538-32T>C MANE Select ENSP00000336725.3:n.538-32T>C
ENST00000336079.7:c.538-32T>C ENSP00000336725.3:n.538-32T>C
ENST00000360160.8:c.538-32T>C ENSP00000353284.4:n.538-32T>C
ENST00000440554.1:c.529-32T>C ENSP00000400377.1:n.529-32T>C
ENST00000454054.5:c.538-32T>C ENSP00000398953.1:n.538-32T>C
ENST00000463199.1:n.56-32T>C
ENST00000469101.1:n.424-32T>C
ENST00000472510.5:n.101-32T>C
NM_001122665.2:c.538-32T>C NP_001116137.1:n.538-32T>C
NM_001302552.1:c.529-32T>C NP_001289481.1:n.529-32T>C
NM_004660.4:c.538-32T>C NP_004651.2:n.538-32T>C
XM_006724878.1:c.538-32T>C XP_006724941.1:n.538-32T>C
XM_011531471.1:c.538-32T>C XP_011529773.1:n.538-32T>C
NM_001122665.3:c.538-32T>C NP_001116137.1:n.538-32T>C
NM_001302552.2:c.529-32T>C NP_001289481.1:n.529-32T>C
NM_001324195.1:c.538-32T>C NP_001311124.1:n.538-32T>C
NR_136716.1:n.689-32T>C
NR_136717.1:n.769-32T>C
NR_136718.1:n.769-32T>C
NR_136719.1:n.559-32T>C
NR_136720.1:n.689-32T>C
NR_136721.1:n.617-32T>C
NR_136722.1:n.684-32T>C
NR_136723.1:n.684-32T>C
NR_136724.1:n.604-32T>C
XR_001756014.2:n.642-32T>C
NM_004660.5:c.538-32T>C MANE Select NP_004651.2:n.538-32T>C
NM_001302552.3:c.529-32T>C NP_001289481.1:n.529-32T>C
NM_001324195.2:c.538-32T>C NP_001311124.1:n.538-32T>C
NR_136716.2:n.607-32T>C
NR_136717.2:n.687-32T>C
NR_136718.2:n.687-32T>C
NR_136719.2:n.477-32T>C
NR_136720.2:n.607-32T>C
NR_136721.2:n.607-32T>C
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