Canonical Allele Identifier: CA4172187
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs768514842
ExAC: 7:17379268 C / G
gnomAD v2: 7-17379268-C-G
gnomAD v3: 7-17339644-C-G
gnomAD v4: 7-17339644-C-G
MyVariant Identifiers: chr7:g.17379268C>G (hg19) chr7:g.17339644C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339644C>G , CM000669.2:g.17339644C>G GRCh38
NC_000007.13:g.17379268C>G , CM000669.1:g.17379268C>G GRCh37
NC_000007.12:g.17345793C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1819C>G MANE Select ENSP00000242057.4:p.Leu607Val
ENST00000637807.1:c.1789C>G ENSP00000490530.1:p.Leu597Val
ENST00000642825.1:c.1774C>G ENSP00000495987.1:p.Leu592Val
ENST00000242057.8:c.1819C>G ENSP00000242057.4:p.Leu607Val
ENST00000463496.1:c.1819C>G ENSP00000436466.1:p.Leu607Val
NM_001621.4:c.1819C>G NP_001612.1:p.Leu607Val
NM_001621.5:c.1819C>G MANE Select NP_001612.1:p.Leu607Val
Search 100 bp 5'
Search 100 bp 3'