Canonical Allele Identifier: CA10436571

Gene: AR

Linked Data

• ClinVar Variation Id: 2932380
• ClinVar RCV Id: RCV003795594
• dbSNP Id: rs754583155
• ExAC: X:66931428 C / T
• gnomAD v2: X-66931428-C-T
• gnomAD v3: X-67711586-C-T
• gnomAD v4: X-67711586-C-T
• COSMIC: COSM5006942 ; COSM5006943
• MyVariant Identifiers: chrX:g.66931428C>T (hg19) ; chrX:g.67711586C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711586C>T , CM000685.2:g.67711586C>T	GRCh38
NC_000023.10:g.66931428C>T , CM000685.1:g.66931428C>T	GRCh37
NC_000023.9:g.66848153C>T	NCBI36
NG_009014.2:g.172555C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*418C>T	ENSP00000379358.4:n.*418C>T
ENST00000374690.9:c.2070C>T MANE Select	ENSP00000363822.3:p.His690=
ENST00000396043.3:c.697C>T	ENSP00000379358.3:n.697C>T
ENST00000396044.8:c.2070C>T	ENSP00000379359.3:p.His690=
ENST00000612452.5:c.2070C>T	ENSP00000484033.2:p.His690=
ENST00000374690.7:c.2070C>T	ENSP00000363822.3:p.His690=
ENST00000396043.2:c.474C>T	ENSP00000379358.2:p.His158=
ENST00000396044.7:c.2070C>T	ENSP00000379359.3:p.His690=
ENST00000612452.4:c.1500C>T	ENSP00000484033.1:p.His500=
NM_000044.3:c.2070C>T	NP_000035.2:p.His690=
NM_001011645.2:c.474C>T	NP_001011645.1:p.His158=
NM_000044.4:c.2070C>T	NP_000035.2:p.His690=
NM_001011645.3:c.474C>T	NP_001011645.1:p.His158=
NM_000044.6:c.2070C>T MANE Select	NP_000035.2:p.His690=