Canonical Allele Identifier: CA4172224
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs573131315
ExAC: 7:17379480 C / T
gnomAD v2: 7-17379480-C-T
gnomAD v4: 7-17339856-C-T
MyVariant Identifiers: chr7:g.17379480C>T (hg19) chr7:g.17339856C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339856C>T , CM000669.2:g.17339856C>T GRCh38
NC_000007.13:g.17379480C>T , CM000669.1:g.17379480C>T GRCh37
NC_000007.12:g.17346005C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2031C>T MANE Select ENSP00000242057.4:p.Asp677=
ENST00000637807.1:c.2001C>T ENSP00000490530.1:p.Asp667=
ENST00000642825.1:c.1986C>T ENSP00000495987.1:p.Asp662=
ENST00000242057.8:c.2031C>T ENSP00000242057.4:p.Asp677=
ENST00000463496.1:c.2031C>T ENSP00000436466.1:p.Asp677=
NM_001621.4:c.2031C>T NP_001612.1:p.Asp677=
NM_001621.5:c.2031C>T MANE Select NP_001612.1:p.Asp677=
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