Canonical Allele Identifier: CA366895757
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs754946915
MyVariant Identifiers: chr7:g.17379478G>C (hg19) chr7:g.17339854G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339854G>C , CM000669.2:g.17339854G>C GRCh38
NC_000007.13:g.17379478G>C , CM000669.1:g.17379478G>C GRCh37
NC_000007.12:g.17346003G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2029G>C MANE Select ENSP00000242057.4:p.Asp677His
ENST00000637807.1:c.1999G>C ENSP00000490530.1:p.Asp667His
ENST00000642825.1:c.1984G>C ENSP00000495987.1:p.Asp662His
ENST00000242057.8:c.2029G>C ENSP00000242057.4:p.Asp677His
ENST00000463496.1:c.2029G>C ENSP00000436466.1:p.Asp677His
NM_001621.4:c.2029G>C NP_001612.1:p.Asp677His
NM_001621.5:c.2029G>C MANE Select NP_001612.1:p.Asp677His
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