Canonical Allele Identifier: CA337722327
Gene: DDX3Y HGNC NCBI

Linked Data

dbSNP Id: rs2032591
MyVariant Identifiers: chrY:g.15030682C>G (hg19) chrY:g.12918770C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12918770C>G , CM000686.2:g.12918770C>G GRCh38
NC_000024.9:g.15030682C>G , CM000686.1:g.15030682C>G GRCh37
NC_000024.8:g.13540076C>G NCBI36
NG_012831.1:g.19664C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336079.8:c.*648C>G MANE Select ENSP00000336725.3:n.*648C>G
ENST00000336079.7:c.*648C>G ENSP00000336725.3:n.*648C>G
NM_004660.4:c.*648C>G NP_004651.2:n.*648C>G
XM_006724878.1:c.*648C>G XP_006724941.1:n.*648C>G
NM_001122665.3:c.*648C>G NP_001116137.1:n.*648C>G
NM_001302552.2:c.*648C>G NP_001289481.1:n.*648C>G
NM_001324195.1:c.*648C>G NP_001311124.1:n.*648C>G
NR_136716.1:n.3100C>G
NR_136717.1:n.2862C>G
NR_136718.1:n.3180C>G
NR_136719.1:n.2970C>G
NR_136720.1:n.3031C>G
NR_136721.1:n.2693C>G
NR_136722.1:n.2777C>G
NR_136723.1:n.3095C>G
NR_136724.1:n.3015C>G
XR_001756014.2:n.2795C>G
NM_004660.5:c.*648C>G MANE Select NP_004651.2:n.*648C>G
NM_001302552.3:c.*648C>G NP_001289481.1:n.*648C>G
NM_001324195.2:c.*648C>G NP_001311124.1:n.*648C>G
NR_136716.2:n.3018C>G
NR_136717.2:n.2780C>G
NR_136718.2:n.3098C>G
NR_136719.2:n.2888C>G
NR_136720.2:n.2949C>G
NR_136721.2:n.2683C>G
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