Canonical Allele Identifier: CA642377529

Gene: AR

Linked Data

• dbSNP Id: rs1225729600
• gnomAD v2: X-66942559-G-T
• gnomAD v3: X-67722717-G-T
• gnomAD v4: X-67722717-G-T
• MyVariant Identifiers: chrX:g.66942559G>T (hg19) ; chrX:g.67722717G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722717G>T , CM000685.2:g.67722717G>T	GRCh38
NC_000023.10:g.66942559G>T , CM000685.1:g.66942559G>T	GRCh37
NC_000023.9:g.66859284G>T	NCBI36
NG_009014.2:g.183686G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*798-110G>T	ENSP00000379358.4:n.*798-110G>T
ENST00000374690.9:c.2450-110G>T MANE Select	ENSP00000363822.3:n.2450-110G>T
ENST00000396043.3:c.1077-110G>T	ENSP00000379358.3:n.1077-110G>T
ENST00000396044.8:c.2174-969G>T	ENSP00000379359.3:n.2174-969G>T
ENST00000612452.5:c.2450-110G>T	ENSP00000484033.2:n.2450-110G>T
ENST00000374690.7:c.2450-110G>T	ENSP00000363822.3:n.2450-110G>T
ENST00000396043.2:c.854-110G>T	ENSP00000379358.2:n.854-110G>T
ENST00000396044.7:c.2174-969G>T	ENSP00000379359.3:n.2174-969G>T
ENST00000612452.4:c.1901-110G>T	ENSP00000484033.1:n.1901-110G>T
NM_000044.3:c.2450-110G>T	NP_000035.2:n.2450-110G>T
NM_001011645.2:c.854-110G>T	NP_001011645.1:n.854-110G>T
NM_000044.4:c.2450-110G>T	NP_000035.2:n.2450-110G>T
NM_001011645.3:c.854-110G>T	NP_001011645.1:n.854-110G>T
NM_000044.6:c.2450-110G>T MANE Select	NP_000035.2:n.2450-110G>T