Canonical Allele Identifier: CA366895168
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs756932231
gnomAD v2: 7-17379226-C-T
gnomAD v4: 7-17339602-C-T
MyVariant Identifiers: chr7:g.17379226C>T (hg19) chr7:g.17339602C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339602C>T , CM000669.2:g.17339602C>T GRCh38
NC_000007.13:g.17379226C>T , CM000669.1:g.17379226C>T GRCh37
NC_000007.12:g.17345751C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1777C>T MANE Select ENSP00000242057.4:p.Pro593Ser
ENST00000637807.1:c.1747C>T ENSP00000490530.1:p.Pro583Ser
ENST00000642825.1:c.1732C>T ENSP00000495987.1:p.Pro578Ser
ENST00000242057.8:c.1777C>T ENSP00000242057.4:p.Pro593Ser
ENST00000463496.1:c.1777C>T ENSP00000436466.1:p.Pro593Ser
NM_001621.4:c.1777C>T NP_001612.1:p.Pro593Ser
NM_001621.5:c.1777C>T MANE Select NP_001612.1:p.Pro593Ser
Search 100 bp 5'
Search 100 bp 3'