Canonical Allele Identifier: CA366895429
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339716-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339716G>T , CM000669.2:g.17339716G>T GRCh38
NC_000007.13:g.17379340G>T , CM000669.1:g.17379340G>T GRCh37
NC_000007.12:g.17345865G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1891G>T MANE Select ENSP00000242057.4:p.Val631Leu
ENST00000637807.1:c.1861G>T ENSP00000490530.1:p.Val621Leu
ENST00000642825.1:c.1846G>T ENSP00000495987.1:p.Val616Leu
ENST00000242057.8:c.1891G>T ENSP00000242057.4:p.Val631Leu
ENST00000463496.1:c.1891G>T ENSP00000436466.1:p.Val631Leu
NM_001621.4:c.1891G>T NP_001612.1:p.Val631Leu
NM_001621.5:c.1891G>T MANE Select NP_001612.1:p.Val631Leu