Canonical Allele Identifier: CA154110019
Gene: AHR HGNC NCBI
COSMIC:
COSN16185295 (not active)
MyVariant.info:
GRCh38 chr7:g.17328796T>C
GRCh37 chr7:g.17368420T>C
gnomAD v2:
7:17368420 T / C
gnomAD v3:
7:17328796 T / C
gnomAD v4:
chr7-17328796-T-C
Joint Max Group AF 0.93265299 (AFR)
Genomes Max Group AF 0.93265299 (AFR)
dbSNP:
2158041
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17328796T>C , CM000669.2:g.17328796T>C GRCh38
NC_000007.13:g.17368420T>C , CM000669.1:g.17368420T>C GRCh37
NC_000007.12:g.17334945T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.450+948T>C MANE Select ENSP00000242057.4:n.450+948T>C
ENST00000637807.1:c.420+948T>C ENSP00000490530.1:n.420+948T>C
ENST00000642825.1:c.405+948T>C ENSP00000495987.1:n.405+948T>C
ENST00000242057.8:c.450+948T>C ENSP00000242057.4:n.450+948T>C
ENST00000463496.1:c.450+948T>C ENSP00000436466.1:n.450+948T>C
NM_001621.4:c.450+948T>C NP_001612.1:n.450+948T>C
NM_001621.5:c.450+948T>C MANE Select NP_001612.1:n.450+948T>C
Search 100 bp 5'
Search 100 bp 3'