Canonical Allele Identifier: CA454134406
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339847-C-T
MyVariant Identifiers: chr7:g.17379471C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339847C>T , CM000669.2:g.17339847C>T GRCh38
NC_000007.13:g.17379471C>T , CM000669.1:g.17379471C>T GRCh37
NC_000007.12:g.17345996C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2022C>T MANE Select ENSP00000242057.4:p.Val674=
ENST00000637807.1:c.1992C>T ENSP00000490530.1:p.Val664=
ENST00000642825.1:c.1977C>T ENSP00000495987.1:p.Val659=
ENST00000242057.8:c.2022C>T ENSP00000242057.4:p.Val674=
ENST00000463496.1:c.2022C>T ENSP00000436466.1:p.Val674=
NM_001621.4:c.2022C>T NP_001612.1:p.Val674=
NM_001621.5:c.2022C>T MANE Select NP_001612.1:p.Val674=
Search 100 bp 5'
Search 100 bp 3'