Canonical Allele Identifier: CA516970616

Gene: AR

Linked Data

• dbSNP Id: rs2076137237
• MyVariant Identifiers: chrX:g.66941687C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721845C>T , CM000685.2:g.67721845C>T	GRCh38
NC_000023.10:g.66941687C>T , CM000685.1:g.66941687C>T	GRCh37
NC_000023.9:g.66858412C>T	NCBI36
NG_009014.2:g.182814C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*679C>T	ENSP00000379358.4:n.*679C>T
ENST00000374690.9:c.2331C>T MANE Select	ENSP00000363822.3:p.His777=
ENST00000396043.3:c.958C>T	ENSP00000379358.3:n.958C>T
ENST00000396044.8:c.2174-1841C>T	ENSP00000379359.3:n.2174-1841C>T
ENST00000612452.5:c.2331C>T	ENSP00000484033.2:p.His777=
ENST00000374690.7:c.2331C>T	ENSP00000363822.3:p.His777=
ENST00000396043.2:c.735C>T	ENSP00000379358.2:p.His245=
ENST00000396044.7:c.2174-1841C>T	ENSP00000379359.3:n.2174-1841C>T
ENST00000612452.4:c.1761C>T	ENSP00000484033.1:p.His587=
NM_000044.3:c.2331C>T	NP_000035.2:p.His777=
NM_001011645.2:c.735C>T	NP_001011645.1:p.His245=
NM_000044.4:c.2331C>T	NP_000035.2:p.His777=
NM_001011645.3:c.735C>T	NP_001011645.1:p.His245=
NM_000044.6:c.2331C>T MANE Select	NP_000035.2:p.His777=