Canonical Allele Identifier: CA1072388299
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI

Linked Data

dbSNP Id: rs1737163275
gnomAD v3: 5-437900-A-G
gnomAD v4: 5-437900-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437900A>G , CM000667.2:g.437900A>G GRCh38
NC_000005.9:g.438015A>G , CM000667.1:g.438015A>G GRCh37
NC_000005.8:g.491015A>G NCBI36
NG_029834.1:g.138725A>G
NG_029834.2:g.138725A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684583.1:c.*3066A>G (AHRR) MANE Select ENSP00000507476.1:n.*3066A>G
ENST00000316418.10:c.*3066A>G (AHRR) ENSP00000323816.6:n.*3066A>G
ENST00000505113.6:c.*5156A>G (PDCD6-AHRR) ENSP00000424601.2:n.*5156A>G
ENST00000675395.1:c.*5210A>G (PDCD6-AHRR) ENSP00000502570.1:n.*5210A>G
ENST00000316418.9:c.*3066A>G (AHRR) ENSP00000323816.5:n.*3066A>G
NM_001242412.1:c.*3066A>G (AHRR) NP_001229341.1:n.*3066A>G
NM_020731.4:c.*3066A>G (AHRR) NP_065782.2:n.*3066A>G
NM_001377236.1:c.*3066A>G (AHRR) MANE Select NP_001364165.1:n.*3066A>G
NM_001377239.1:c.*3066A>G (AHRR) NP_001364168.1:n.*3066A>G
NR_165159.2:n.5507A>G (PDCD6-AHRR)
NR_165163.2:n.5453A>G (PDCD6-AHRR)