Canonical Allele Identifier: CA454134192
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs747196573
gnomAD v4: 7-17339646-G-C
MyVariant Identifiers: chr7:g.17379270G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339646G>C , CM000669.2:g.17339646G>C GRCh38
NC_000007.13:g.17379270G>C , CM000669.1:g.17379270G>C GRCh37
NC_000007.12:g.17345795G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1821G>C MANE Select ENSP00000242057.4:p.Leu607=
ENST00000637807.1:c.1791G>C ENSP00000490530.1:p.Leu597=
ENST00000642825.1:c.1776G>C ENSP00000495987.1:p.Leu592=
ENST00000242057.8:c.1821G>C ENSP00000242057.4:p.Leu607=
ENST00000463496.1:c.1821G>C ENSP00000436466.1:p.Leu607=
NM_001621.4:c.1821G>C NP_001612.1:p.Leu607=
NM_001621.5:c.1821G>C MANE Select NP_001612.1:p.Leu607=
Search 100 bp 5'
Search 100 bp 3'