Canonical Allele Identifier: CA366895536
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1269780039
gnomAD v2: 7-17379384-G-T
gnomAD v4: 7-17339760-G-T
MyVariant Identifiers: chr7:g.17379384G>T (hg19) chr7:g.17339760G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339760G>T , CM000669.2:g.17339760G>T GRCh38
NC_000007.13:g.17379384G>T , CM000669.1:g.17379384G>T GRCh37
NC_000007.12:g.17345909G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1935G>T MANE Select ENSP00000242057.4:p.Met645Ile
ENST00000637807.1:c.1905G>T ENSP00000490530.1:p.Met635Ile
ENST00000642825.1:c.1890G>T ENSP00000495987.1:p.Met630Ile
ENST00000242057.8:c.1935G>T ENSP00000242057.4:p.Met645Ile
ENST00000463496.1:c.1935G>T ENSP00000436466.1:p.Met645Ile
NM_001621.4:c.1935G>T NP_001612.1:p.Met645Ile
NM_001621.5:c.1935G>T MANE Select NP_001612.1:p.Met645Ile
Search 100 bp 5'
Search 100 bp 3'