Canonical Allele Identifier: CA642472686

Gene: AR

Linked Data

• dbSNP Id: rs1244023584
• gnomAD v2: X-66764948-G-C
• gnomAD v4: X-67545106-G-C
• MyVariant Identifiers: chrX:g.66764948G>C (hg19) ; chrX:g.67545106G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545106G>C , CM000685.2:g.67545106G>C	GRCh38
NC_000023.10:g.66764948G>C , CM000685.1:g.66764948G>C	GRCh37
NC_000023.9:g.66681673G>C	NCBI36
NG_009014.2:g.6075G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.-41G>C	ENSP00000379358.4:n.-41G>C
ENST00000374690.9:c.-41G>C MANE Select	ENSP00000363822.3:n.-41G>C
ENST00000612452.5:c.-41G>C	ENSP00000484033.2:n.-41G>C
ENST00000374690.7:c.-41G>C	ENSP00000363822.3:n.-41G>C
ENST00000396044.7:c.-41G>C	ENSP00000379359.3:n.-41G>C
ENST00000504326.5:c.-41G>C	ENSP00000421155.1:n.-41G>C
ENST00000513847.5:n.287G>C
ENST00000514029.5:c.-41G>C	ENSP00000425199.1:n.-41G>C
ENST00000612010.4:c.-41G>C	ENSP00000482407.1:n.-41G>C
ENST00000612452.4:c.-611G>C	ENSP00000484033.1:n.-611G>C
ENST00000613054.2:c.-41G>C	ENSP00000479013.1:n.-41G>C
NM_000044.3:c.-41G>C	NP_000035.2:n.-41G>C
NM_000044.4:c.-41G>C	NP_000035.2:n.-41G>C
NM_001011645.3:c.-1824G>C	NP_001011645.1:n.-1824G>C
NM_001348061.1:c.-41G>C	NP_001334990.1:n.-41G>C
NM_001348063.1:c.-41G>C	NP_001334992.1:n.-41G>C
NM_001348064.1:c.-41G>C	NP_001334993.1:n.-41G>C
NM_000044.6:c.-41G>C MANE Select	NP_000035.2:n.-41G>C