Canonical Allele Identifier: CA366895564
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs757525465
gnomAD v2: 7-17379397-A-C
gnomAD v4: 7-17339773-A-C
MyVariant Identifiers: chr7:g.17379397A>C (hg19) chr7:g.17339773A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339773A>C , CM000669.2:g.17339773A>C GRCh38
NC_000007.13:g.17379397A>C , CM000669.1:g.17379397A>C GRCh37
NC_000007.12:g.17345922A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1948A>C MANE Select ENSP00000242057.4:p.Met650Leu
ENST00000637807.1:c.1918A>C ENSP00000490530.1:p.Met640Leu
ENST00000642825.1:c.1903A>C ENSP00000495987.1:p.Met635Leu
ENST00000242057.8:c.1948A>C ENSP00000242057.4:p.Met650Leu
ENST00000463496.1:c.1948A>C ENSP00000436466.1:p.Met650Leu
NM_001621.4:c.1948A>C NP_001612.1:p.Met650Leu
NM_001621.5:c.1948A>C MANE Select NP_001612.1:p.Met650Leu
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