Canonical Allele Identifier: CA10436300
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs370893700
gnomAD v2: X-66765620-C-G
gnomAD v3: X-67545778-C-G
gnomAD v4: X-67545778-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545778C>G , CM000685.2:g.67545778C>G GRCh38
NC_000023.10:g.66765620C>G , CM000685.1:g.66765620C>G GRCh37
NC_000023.9:g.66682345C>G NCBI36
NG_009014.2:g.6747C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.632C>G ENSP00000379358.4:p.Ala211Gly
ENST00000374690.9:c.632C>G MANE Select ENSP00000363822.3:p.Ala211Gly
ENST00000396044.8:c.632C>G ENSP00000379359.3:p.Ala211Gly
ENST00000612452.5:c.632C>G ENSP00000484033.2:p.Ala211Gly
ENST00000374690.7:c.632C>G ENSP00000363822.3:p.Ala211Gly
ENST00000396044.7:c.632C>G ENSP00000379359.3:p.Ala211Gly
ENST00000504326.5:c.632C>G ENSP00000421155.1:p.Ala211Gly
ENST00000513847.5:n.959C>G
ENST00000514029.5:c.632C>G ENSP00000425199.1:p.Ala211Gly
ENST00000612010.4:c.632C>G ENSP00000482407.1:p.Ala211Gly
ENST00000612452.4:c.62C>G ENSP00000484033.1:p.Ala21Gly
ENST00000613054.2:c.632C>G ENSP00000479013.1:p.Ala211Gly
NM_000044.3:c.632C>G NP_000035.2:p.Ala211Gly
NM_000044.4:c.632C>G NP_000035.2:p.Ala211Gly
NM_001011645.3:c.-1152C>G NP_001011645.1:n.-1152C>G
NM_001348061.1:c.632C>G NP_001334990.1:p.Ala211Gly
NM_001348063.1:c.632C>G NP_001334992.1:p.Ala211Gly
NM_001348064.1:c.632C>G NP_001334993.1:p.Ala211Gly
NM_000044.6:c.632C>G MANE Select NP_000035.2:p.Ala211Gly