Canonical Allele Identifier: CA877563418

Gene: AR

Linked Data

• dbSNP Id: rs1159693853
• gnomAD v3: X-67711239-C-T
• gnomAD v4: X-67711239-C-T
• MyVariant Identifiers: chrX:g.66931081C>T (hg19) ; chrX:g.67711239C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711239C>T , CM000685.2:g.67711239C>T	GRCh38
NC_000023.10:g.66931081C>T , CM000685.1:g.66931081C>T	GRCh37
NC_000023.9:g.66847806C>T	NCBI36
NG_009014.2:g.172208C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*234-163C>T	ENSP00000379358.4:n.*234-163C>T
ENST00000374690.9:c.1886-163C>T MANE Select	ENSP00000363822.3:n.1886-163C>T
ENST00000396043.3:c.513-163C>T	ENSP00000379358.3:n.513-163C>T
ENST00000396044.8:c.1886-163C>T	ENSP00000379359.3:n.1886-163C>T
ENST00000612452.5:c.1886-163C>T	ENSP00000484033.2:n.1886-163C>T
ENST00000374690.7:c.1886-163C>T	ENSP00000363822.3:n.1886-163C>T
ENST00000396043.2:c.290-163C>T	ENSP00000379358.2:n.290-163C>T
ENST00000396044.7:c.1886-163C>T	ENSP00000379359.3:n.1886-163C>T
ENST00000612452.4:c.1316-163C>T	ENSP00000484033.1:n.1316-163C>T
NM_000044.3:c.1886-163C>T	NP_000035.2:n.1886-163C>T
NM_001011645.2:c.290-163C>T	NP_001011645.1:n.290-163C>T
NM_000044.4:c.1886-163C>T	NP_000035.2:n.1886-163C>T
NM_001011645.3:c.290-163C>T	NP_001011645.1:n.290-163C>T
NM_000044.6:c.1886-163C>T MANE Select	NP_000035.2:n.1886-163C>T