Canonical Allele Identifier: CA516970594

Gene: AR

Linked Data

• dbSNP Id: rs2076137217
• MyVariant Identifiers: chrX:g.66941681C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721839C>G , CM000685.2:g.67721839C>G	GRCh38
NC_000023.10:g.66941681C>G , CM000685.1:g.66941681C>G	GRCh37
NC_000023.9:g.66858406C>G	NCBI36
NG_009014.2:g.182808C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*673C>G	ENSP00000379358.4:n.*673C>G
ENST00000374690.9:c.2325C>G MANE Select	ENSP00000363822.3:p.Arg775=
ENST00000396043.3:c.952C>G	ENSP00000379358.3:n.952C>G
ENST00000396044.8:c.2174-1847C>G	ENSP00000379359.3:n.2174-1847C>G
ENST00000612452.5:c.2325C>G	ENSP00000484033.2:p.Arg775=
ENST00000374690.7:c.2325C>G	ENSP00000363822.3:p.Arg775=
ENST00000396043.2:c.729C>G	ENSP00000379358.2:p.Arg243=
ENST00000396044.7:c.2174-1847C>G	ENSP00000379359.3:n.2174-1847C>G
ENST00000612452.4:c.1755C>G	ENSP00000484033.1:p.Arg585=
NM_000044.3:c.2325C>G	NP_000035.2:p.Arg775=
NM_001011645.2:c.729C>G	NP_001011645.1:p.Arg243=
NM_000044.4:c.2325C>G	NP_000035.2:p.Arg775=
NM_001011645.3:c.729C>G	NP_001011645.1:p.Arg243=
NM_000044.6:c.2325C>G MANE Select	NP_000035.2:p.Arg775=