Canonical Allele Identifier: CA516970345

Gene: AR

Linked Data

• dbSNP Id: rs2147530718
• MyVariant Identifiers: chrX:g.66937354T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717512T>C , CM000685.2:g.67717512T>C	GRCh38
NC_000023.10:g.66937354T>C , CM000685.1:g.66937354T>C	GRCh37
NC_000023.9:g.66854079T>C	NCBI36
NG_009014.2:g.178481T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*556T>C	ENSP00000379358.4:n.*556T>C
ENST00000374690.9:c.2208T>C MANE Select	ENSP00000363822.3:p.Ala736=
ENST00000396043.3:c.835T>C	ENSP00000379358.3:n.835T>C
ENST00000396044.8:c.2173+5823T>C	ENSP00000379359.3:n.2173+5823T>C
ENST00000612452.5:c.2208T>C	ENSP00000484033.2:p.Ala736=
ENST00000374690.7:c.2208T>C	ENSP00000363822.3:p.Ala736=
ENST00000396043.2:c.612T>C	ENSP00000379358.2:p.Ala204=
ENST00000396044.7:c.2173+5823T>C	ENSP00000379359.3:n.2173+5823T>C
ENST00000612452.4:c.1638T>C	ENSP00000484033.1:p.Ala546=
NM_000044.3:c.2208T>C	NP_000035.2:p.Ala736=
NM_001011645.2:c.612T>C	NP_001011645.1:p.Ala204=
NM_000044.4:c.2208T>C	NP_000035.2:p.Ala736=
NM_001011645.3:c.612T>C	NP_001011645.1:p.Ala204=
NM_000044.6:c.2208T>C MANE Select	NP_000035.2:p.Ala736=