Canonical Allele Identifier: CA366895642
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339804-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339804T>C , CM000669.2:g.17339804T>C GRCh38
NC_000007.13:g.17379428T>C , CM000669.1:g.17379428T>C GRCh37
NC_000007.12:g.17345953T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1979T>C MANE Select ENSP00000242057.4:p.Val660Ala
ENST00000637807.1:c.1949T>C ENSP00000490530.1:p.Val650Ala
ENST00000642825.1:c.1934T>C ENSP00000495987.1:p.Val645Ala
ENST00000242057.8:c.1979T>C ENSP00000242057.4:p.Val660Ala
ENST00000463496.1:c.1979T>C ENSP00000436466.1:p.Val660Ala
NM_001621.4:c.1979T>C NP_001612.1:p.Val660Ala
NM_001621.5:c.1979T>C MANE Select NP_001612.1:p.Val660Ala