Canonical Allele Identifier: CA2435134790

Gene: AR

Linked Data

• ClinVar Variation Id: 2948938
• ClinVar RCV Id: RCV003801664
• dbSNP Id: rs2076141638
• gnomAD v4: X-67722819-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722819C>T , CM000685.2:g.67722819C>T	GRCh38
NC_000023.10:g.66942661C>T , CM000685.1:g.66942661C>T	GRCh37
NC_000023.9:g.66859386C>T	NCBI36
NG_009014.2:g.183788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*798-8C>T	ENSP00000379358.4:n.*798-8C>T
ENST00000374690.9:c.2450-8C>T MANE Select	ENSP00000363822.3:n.2450-8C>T
ENST00000396043.3:c.1077-8C>T	ENSP00000379358.3:n.1077-8C>T
ENST00000396044.8:c.2174-867C>T	ENSP00000379359.3:n.2174-867C>T
ENST00000612452.5:c.2450-8C>T	ENSP00000484033.2:n.2450-8C>T
ENST00000374690.7:c.2450-8C>T	ENSP00000363822.3:n.2450-8C>T
ENST00000396043.2:c.854-8C>T	ENSP00000379358.2:n.854-8C>T
ENST00000396044.7:c.2174-867C>T	ENSP00000379359.3:n.2174-867C>T
ENST00000612452.4:c.1901-8C>T	ENSP00000484033.1:n.1901-8C>T
NM_000044.3:c.2450-8C>T	NP_000035.2:n.2450-8C>T
NM_001011645.2:c.854-8C>T	NP_001011645.1:n.854-8C>T
NM_000044.4:c.2450-8C>T	NP_000035.2:n.2450-8C>T
NM_001011645.3:c.854-8C>T	NP_001011645.1:n.854-8C>T
NM_000044.6:c.2450-8C>T MANE Select	NP_000035.2:n.2450-8C>T