Canonical Allele Identifier: CA877566072

Gene: AR

Linked Data

• dbSNP Id: rs1284434419
• gnomAD v3: X-67721809-T-C
• gnomAD v4: X-67721809-T-C
• MyVariant Identifiers: chrX:g.66941651T>C (hg19) ; chrX:g.67721809T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721809T>C , CM000685.2:g.67721809T>C	GRCh38
NC_000023.10:g.66941651T>C , CM000685.1:g.66941651T>C	GRCh37
NC_000023.9:g.66858376T>C	NCBI36
NG_009014.2:g.182778T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*667-24T>C	ENSP00000379358.4:n.*667-24T>C
ENST00000374690.9:c.2319-24T>C MANE Select	ENSP00000363822.3:n.2319-24T>C
ENST00000396043.3:c.946-24T>C	ENSP00000379358.3:n.946-24T>C
ENST00000396044.8:c.2174-1877T>C	ENSP00000379359.3:n.2174-1877T>C
ENST00000612452.5:c.2319-24T>C	ENSP00000484033.2:n.2319-24T>C
ENST00000374690.7:c.2319-24T>C	ENSP00000363822.3:n.2319-24T>C
ENST00000396043.2:c.723-24T>C	ENSP00000379358.2:n.723-24T>C
ENST00000396044.7:c.2174-1877T>C	ENSP00000379359.3:n.2174-1877T>C
ENST00000612452.4:c.1749-24T>C	ENSP00000484033.1:n.1749-24T>C
NM_000044.3:c.2319-24T>C	NP_000035.2:n.2319-24T>C
NM_001011645.2:c.723-24T>C	NP_001011645.1:n.723-24T>C
NM_000044.4:c.2319-24T>C	NP_000035.2:n.2319-24T>C
NM_001011645.3:c.723-24T>C	NP_001011645.1:n.723-24T>C
NM_000044.6:c.2319-24T>C MANE Select	NP_000035.2:n.2319-24T>C