Canonical Allele Identifier: CA10602648
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 268093
ClinVar RCV Id: RCV000258807
dbSNP Id: rs886041050
MyVariant Identifiers: chrX:g.66863166T>C (hg19) chrX:g.67643324T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67643324T>C , CM000685.2:g.67643324T>C GRCh38
NC_000023.10:g.66863166T>C , CM000685.1:g.66863166T>C GRCh37
NC_000023.9:g.66779891T>C NCBI36
NG_009014.2:g.104293T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*33T>C ENSP00000379358.4:n.*33T>C
ENST00000374690.9:c.1685T>C MANE Select ENSP00000363822.3:p.Ile562Thr
ENST00000396043.3:c.312T>C ENSP00000379358.3:n.312T>C
ENST00000396044.8:c.1685T>C ENSP00000379359.3:p.Ile562Thr
ENST00000612452.5:c.1685T>C ENSP00000484033.2:p.Ile562Thr
ENST00000374690.7:c.1685T>C ENSP00000363822.3:p.Ile562Thr
ENST00000396043.2:c.89T>C ENSP00000379358.2:p.Ile30Thr
ENST00000396044.7:c.1685T>C ENSP00000379359.3:p.Ile562Thr
ENST00000504326.5:c.1685T>C ENSP00000421155.1:p.Ile562Thr
ENST00000513847.5:n.2012T>C
ENST00000514029.5:c.1685T>C ENSP00000425199.1:p.Ile562Thr
ENST00000612010.4:c.1685T>C ENSP00000482407.1:p.Ile562Thr
ENST00000612452.4:c.1115T>C ENSP00000484033.1:p.Ile372Thr
ENST00000613054.2:c.1617-42617T>C ENSP00000479013.1:n.1617-42617T>C
NM_000044.3:c.1685T>C NP_000035.2:p.Ile562Thr
NM_001011645.2:c.89T>C NP_001011645.1:p.Ile30Thr
NM_000044.4:c.1685T>C NP_000035.2:p.Ile562Thr
NM_001011645.3:c.89T>C NP_001011645.1:p.Ile30Thr
NM_001348061.1:c.1685T>C NP_001334990.1:p.Ile562Thr
NM_001348063.1:c.1685T>C NP_001334992.1:p.Ile562Thr
NM_001348064.1:c.1617-42617T>C NP_001334993.1:n.1617-42617T>C
NM_000044.6:c.1685T>C MANE Select NP_000035.2:p.Ile562Thr
Search 100 bp 5'
Search 100 bp 3'