Canonical Allele Identifier: CA10436387

Gene: AR

Linked Data

• ClinVar Variation Id: 2925049
• ClinVar RCV Id: RCV003780703
• dbSNP Id: rs752328862
• ExAC: X:66766134 T / C
• gnomAD v2: X-66766134-T-C
• gnomAD v3: X-67546292-T-C
• gnomAD v4: X-67546292-T-C
• MyVariant Identifiers: chrX:g.66766134T>C (hg19) ; chrX:g.67546292T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67546292T>C , CM000685.2:g.67546292T>C	GRCh38
NC_000023.10:g.66766134T>C , CM000685.1:g.66766134T>C	GRCh37
NC_000023.9:g.66682859T>C	NCBI36
NG_009014.2:g.7261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.1146T>C	ENSP00000379358.4:p.His382=
ENST00000374690.9:c.1146T>C MANE Select	ENSP00000363822.3:p.His382=
ENST00000396044.8:c.1146T>C	ENSP00000379359.3:p.His382=
ENST00000612452.5:c.1146T>C	ENSP00000484033.2:p.His382=
ENST00000374690.7:c.1146T>C	ENSP00000363822.3:p.His382=
ENST00000396044.7:c.1146T>C	ENSP00000379359.3:p.His382=
ENST00000504326.5:c.1146T>C	ENSP00000421155.1:p.His382=
ENST00000513847.5:n.1473T>C
ENST00000514029.5:c.1146T>C	ENSP00000425199.1:p.His382=
ENST00000612010.4:c.1146T>C	ENSP00000482407.1:p.His382=
ENST00000612452.4:c.576T>C	ENSP00000484033.1:p.His192=
ENST00000613054.2:c.1146T>C	ENSP00000479013.1:p.His382=
NM_000044.3:c.1146T>C	NP_000035.2:p.His382=
NM_000044.4:c.1146T>C	NP_000035.2:p.His382=
NM_001011645.3:c.-638T>C	NP_001011645.1:n.-638T>C
NM_001348061.1:c.1146T>C	NP_001334990.1:p.His382=
NM_001348063.1:c.1146T>C	NP_001334992.1:p.His382=
NM_001348064.1:c.1146T>C	NP_001334993.1:p.His382=
NM_000044.6:c.1146T>C MANE Select	NP_000035.2:p.His382=