Canonical Allele Identifier: CA4172199
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs767197872
gnomAD v2: 7-17379334-C-G
gnomAD v4: 7-17339710-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339710C>G , CM000669.2:g.17339710C>G GRCh38
NC_000007.13:g.17379334C>G , CM000669.1:g.17379334C>G GRCh37
NC_000007.12:g.17345859C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1885C>G MANE Select ENSP00000242057.4:p.Gln629Glu
ENST00000637807.1:c.1855C>G ENSP00000490530.1:p.Gln619Glu
ENST00000642825.1:c.1840C>G ENSP00000495987.1:p.Gln614Glu
ENST00000242057.8:c.1885C>G ENSP00000242057.4:p.Gln629Glu
ENST00000463496.1:c.1885C>G ENSP00000436466.1:p.Gln629Glu
NM_001621.4:c.1885C>G NP_001612.1:p.Gln629Glu
NM_001621.5:c.1885C>G MANE Select NP_001612.1:p.Gln629Glu