Canonical Allele Identifier: CA120740
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9832
ClinVar RCV Id: RCV000010506
dbSNP Id: rs137852579
MyVariant Identifiers: chrX:g.66931391T>C (hg19) chrX:g.67711549T>C (hg38)
PubMed: PMID:4061484 PMID:7537149
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67711549T>C , CM000685.2:g.67711549T>C GRCh38
NC_000023.10:g.66931391T>C , CM000685.1:g.66931391T>C GRCh37
NC_000023.9:g.66848116T>C NCBI36
NG_009014.2:g.172518T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*381T>C ENSP00000379358.4:n.*381T>C
ENST00000374690.9:c.2033T>C MANE Select ENSP00000363822.3:p.Leu678Pro
ENST00000396043.3:c.660T>C ENSP00000379358.3:n.660T>C
ENST00000396044.8:c.2033T>C ENSP00000379359.3:p.Leu678Pro
ENST00000612452.5:c.2033T>C ENSP00000484033.2:p.Leu678Pro
ENST00000374690.7:c.2033T>C ENSP00000363822.3:p.Leu678Pro
ENST00000396043.2:c.437T>C ENSP00000379358.2:p.Leu146Pro
ENST00000396044.7:c.2033T>C ENSP00000379359.3:p.Leu678Pro
ENST00000612452.4:c.1463T>C ENSP00000484033.1:p.Leu488Pro
NM_000044.3:c.2033T>C NP_000035.2:p.Leu678Pro
NM_001011645.2:c.437T>C NP_001011645.1:p.Leu146Pro
NM_000044.4:c.2033T>C NP_000035.2:p.Leu678Pro
NM_001011645.3:c.437T>C NP_001011645.1:p.Leu146Pro
NM_000044.6:c.2033T>C MANE Select NP_000035.2:p.Leu678Pro
Search 100 bp 5'
Search 100 bp 3'