Canonical Allele Identifier: CA366895160
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339598-G-C
MyVariant Identifiers: chr7:g.17379222G>C (hg19) chr7:g.17339598G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339598G>C , CM000669.2:g.17339598G>C GRCh38
NC_000007.13:g.17379222G>C , CM000669.1:g.17379222G>C GRCh37
NC_000007.12:g.17345747G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1773G>C MANE Select ENSP00000242057.4:p.Lys591Asn
ENST00000637807.1:c.1743G>C ENSP00000490530.1:p.Lys581Asn
ENST00000642825.1:c.1728G>C ENSP00000495987.1:p.Lys576Asn
ENST00000242057.8:c.1773G>C ENSP00000242057.4:p.Lys591Asn
ENST00000463496.1:c.1773G>C ENSP00000436466.1:p.Lys591Asn
NM_001621.4:c.1773G>C NP_001612.1:p.Lys591Asn
NM_001621.5:c.1773G>C MANE Select NP_001612.1:p.Lys591Asn
Search 100 bp 5'
Search 100 bp 3'