Canonical Allele Identifier: CA413423341

Gene: AR

Linked Data

• dbSNP Id: rs1602272594
• MyVariant Identifiers: chrX:g.66931426C>T (hg19) ; chrX:g.67711584C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711584C>T , CM000685.2:g.67711584C>T	GRCh38
NC_000023.10:g.66931426C>T , CM000685.1:g.66931426C>T	GRCh37
NC_000023.9:g.66848151C>T	NCBI36
NG_009014.2:g.172553C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*416C>T	ENSP00000379358.4:n.*416C>T
ENST00000374690.9:c.2068C>T MANE Select	ENSP00000363822.3:p.His690Tyr
ENST00000396043.3:c.695C>T	ENSP00000379358.3:n.695C>T
ENST00000396044.8:c.2068C>T	ENSP00000379359.3:p.His690Tyr
ENST00000612452.5:c.2068C>T	ENSP00000484033.2:p.His690Tyr
ENST00000374690.7:c.2068C>T	ENSP00000363822.3:p.His690Tyr
ENST00000396043.2:c.472C>T	ENSP00000379358.2:p.His158Tyr
ENST00000396044.7:c.2068C>T	ENSP00000379359.3:p.His690Tyr
ENST00000612452.4:c.1498C>T	ENSP00000484033.1:p.His500Tyr
NM_000044.3:c.2068C>T	NP_000035.2:p.His690Tyr
NM_001011645.2:c.472C>T	NP_001011645.1:p.His158Tyr
NM_000044.4:c.2068C>T	NP_000035.2:p.His690Tyr
NM_001011645.3:c.472C>T	NP_001011645.1:p.His158Tyr
NM_000044.6:c.2068C>T MANE Select	NP_000035.2:p.His690Tyr