Canonical Allele Identifier: CA120761
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9839
ClinVar RCV Id: RCV000010513
dbSNP Id: rs137852587
MyVariant Identifiers: chrX:g.66863229T>A (hg19) chrX:g.67643387T>A (hg38)
PubMed: PMID:3216866 PMID:8809734
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67643387T>A , CM000685.2:g.67643387T>A GRCh38
NC_000023.10:g.66863229T>A , CM000685.1:g.66863229T>A GRCh37
NC_000023.9:g.66779954T>A NCBI36
NG_009014.2:g.104356T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*96T>A ENSP00000379358.4:n.*96T>A
ENST00000374690.9:c.1748T>A MANE Select ENSP00000363822.3:p.Phe583Tyr
ENST00000396043.3:c.375T>A ENSP00000379358.3:n.375T>A
ENST00000396044.8:c.1748T>A ENSP00000379359.3:p.Phe583Tyr
ENST00000612452.5:c.1748T>A ENSP00000484033.2:p.Phe583Tyr
ENST00000374690.7:c.1748T>A ENSP00000363822.3:p.Phe583Tyr
ENST00000396043.2:c.152T>A ENSP00000379358.2:p.Phe51Tyr
ENST00000396044.7:c.1748T>A ENSP00000379359.3:p.Phe583Tyr
ENST00000504326.5:c.1748T>A ENSP00000421155.1:p.Phe583Tyr
ENST00000513847.5:n.2075T>A
ENST00000514029.5:c.1748T>A ENSP00000425199.1:p.Phe583Tyr
ENST00000612010.4:c.1748T>A ENSP00000482407.1:p.Phe583Tyr
ENST00000612452.4:c.1178T>A ENSP00000484033.1:p.Phe393Tyr
ENST00000613054.2:c.1617-42554T>A ENSP00000479013.1:n.1617-42554T>A
NM_000044.3:c.1748T>A NP_000035.2:p.Phe583Tyr
NM_001011645.2:c.152T>A NP_001011645.1:p.Phe51Tyr
NM_000044.4:c.1748T>A NP_000035.2:p.Phe583Tyr
NM_001011645.3:c.152T>A NP_001011645.1:p.Phe51Tyr
NM_001348061.1:c.1748T>A NP_001334990.1:p.Phe583Tyr
NM_001348063.1:c.1748T>A NP_001334992.1:p.Phe583Tyr
NM_001348064.1:c.1617-42554T>A NP_001334993.1:n.1617-42554T>A
NM_000044.6:c.1748T>A MANE Select NP_000035.2:p.Phe583Tyr
Search 100 bp 5'
Search 100 bp 3'