Canonical Allele Identifier: CA15373084
Gene: AHRR HGNC NCBI
PDCD6-AHRR HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.437987G>T
GRCh37 chr5:g.438102G>T
gnomAD v2:
5:438102 G / T
gnomAD v3:
5:437987 G / T
gnomAD v4:
chr5-437987-G-T
Joint Max Group AF 0.78285049 (NFE)
Genomes Max Group AF 0.78285049 (NFE)
Exomes Max Group AF 0.60305639 (EAS)
dbSNP:
10078
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.437987G>T , CM000667.2:g.437987G>T GRCh38
NC_000005.9:g.438102G>T , CM000667.1:g.438102G>T GRCh37
NC_000005.8:g.491102G>T NCBI36
NG_029834.1:g.138812G>T
NG_029834.2:g.138812G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684583.1:c.*3153G>T (AHRR) MANE Select ENSP00000507476.1:n.*3153G>T
ENST00000316418.10:c.*3153G>T (AHRR) ENSP00000323816.6:n.*3153G>T
ENST00000505113.6:c.*5243G>T (PDCD6-AHRR) ENSP00000424601.2:n.*5243G>T
ENST00000675395.1:c.*5297G>T (PDCD6-AHRR) ENSP00000502570.1:n.*5297G>T
ENST00000316418.9:c.*3153G>T (AHRR) ENSP00000323816.5:n.*3153G>T
NM_001242412.1:c.*3153G>T (AHRR) NP_001229341.1:n.*3153G>T
NM_020731.4:c.*3153G>T (AHRR) NP_065782.2:n.*3153G>T
NM_001377236.1:c.*3153G>T (AHRR) MANE Select NP_001364165.1:n.*3153G>T
NM_001377239.1:c.*3153G>T (AHRR) NP_001364168.1:n.*3153G>T
NR_165159.2:n.5594G>T (PDCD6-AHRR)
NR_165163.2:n.5540G>T (PDCD6-AHRR)
Search 100 bp 5'
Search 100 bp 3'