Canonical Allele Identifier: CA15373084
Gene: AHRR HGNC NCBI

Linked Data

dbSNP Id: rs10078

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
ENST00000316418.10:c.*3153G>T ENSP00000323816.6:p.=
ENST00000505113.6:c.*5243G>T ENSP00000424601.2:p.=
ENST00000675395.1:c.*5297G>T ENSP00000502570.1:p.=
ENST00000316418.9:c.*3153G>T ENSP00000323816.5:p.=
NM_001242412.1:c.*3153G>T NP_001229341.1:p.=
NM_020731.4:c.*3153G>T NP_065782.2:p.=
NM_001377236.1:c.*3153G>T MANE Select NP_001364165.1:p.=
NM_001377239.1:c.*3153G>T NP_001364168.1:p.=
NR_165159.2:n.5594G>T
NR_165163.2:n.5540G>T