Canonical Allele Identifier: CA337722085
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs9341285
gnomAD v3: Y-12905594-C-T
gnomAD v4: Y-12905594-C-T
MyVariant Identifiers: chrY:g.15017505C>T (hg19) chrY:g.12905594C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12905594C>T , CM000686.2:g.12905594C>T GRCh38
NC_000024.9:g.15017505C>T , CM000686.1:g.15017505C>T GRCh37
NC_000024.8:g.13526899C>T NCBI36
NG_012831.1:g.6487C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.45+613C>T MANE Select ENSP00000336725.3:n.45+613C>T
ENST00000336079.7:c.45+613C>T ENSP00000336725.3:n.45+613C>T
ENST00000360160.8:c.45+613C>T ENSP00000353284.4:n.45+613C>T
ENST00000454054.5:c.45+613C>T ENSP00000398953.1:n.45+613C>T
ENST00000493363.1:n.133+613C>T
NM_001122665.2:c.45+613C>T NP_001116137.1:n.45+613C>T
NM_004660.4:c.45+613C>T NP_004651.2:n.45+613C>T
XM_006724878.1:c.45+613C>T XP_006724941.1:n.45+613C>T
XM_011531471.1:c.45+613C>T XP_011529773.1:n.45+613C>T
NM_001122665.3:c.45+613C>T NP_001116137.1:n.45+613C>T
NM_001324195.1:c.45+613C>T NP_001311124.1:n.45+613C>T
NR_136716.1:n.196+613C>T
NR_136717.1:n.196+613C>T
NR_136718.1:n.196+613C>T
NR_136719.1:n.196+613C>T
NR_136720.1:n.196+613C>T
NR_136721.1:n.124+613C>T
XR_001756014.2:n.149+613C>T
NM_004660.5:c.45+613C>T MANE Select NP_004651.2:n.45+613C>T
NM_001324195.2:c.45+613C>T NP_001311124.1:n.45+613C>T
NR_136716.2:n.114+613C>T
NR_136717.2:n.114+613C>T
NR_136718.2:n.114+613C>T
NR_136719.2:n.114+613C>T
NR_136720.2:n.114+613C>T
NR_136721.2:n.114+613C>T
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