Canonical Allele Identifier: CA413427050

Gene: AR

Linked Data

• dbSNP Id: rs2147536049
• MyVariant Identifiers: chrX:g.66941790C>G (hg19) ; chrX:g.67721948C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721948C>G , CM000685.2:g.67721948C>G	GRCh38
NC_000023.10:g.66941790C>G , CM000685.1:g.66941790C>G	GRCh37
NC_000023.9:g.66858515C>G	NCBI36
NG_009014.2:g.182917C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*782C>G	ENSP00000379358.4:n.*782C>G
ENST00000374690.9:c.2434C>G MANE Select	ENSP00000363822.3:p.Leu812Val
ENST00000396043.3:c.1061C>G	ENSP00000379358.3:n.1061C>G
ENST00000396044.8:c.2174-1738C>G	ENSP00000379359.3:n.2174-1738C>G
ENST00000612452.5:c.2434C>G	ENSP00000484033.2:p.Leu812Val
ENST00000374690.7:c.2434C>G	ENSP00000363822.3:p.Leu812Val
ENST00000396043.2:c.838C>G	ENSP00000379358.2:p.Leu280Val
ENST00000396044.7:c.2174-1738C>G	ENSP00000379359.3:n.2174-1738C>G
ENST00000612452.4:c.1864C>G	ENSP00000484033.1:p.Leu622Val
NM_000044.3:c.2434C>G	NP_000035.2:p.Leu812Val
NM_001011645.2:c.838C>G	NP_001011645.1:p.Leu280Val
NM_000044.4:c.2434C>G	NP_000035.2:p.Leu812Val
NM_001011645.3:c.838C>G	NP_001011645.1:p.Leu280Val
NM_000044.6:c.2434C>G MANE Select	NP_000035.2:p.Leu812Val