Canonical Allele Identifier: CA366895547
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1992818
ClinVar RCV Id: RCV002814462
MyVariant Identifiers: chr7:g.17379388G>C (hg19) chr7:g.17339764G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339764G>C , CM000669.2:g.17339764G>C GRCh38
NC_000007.13:g.17379388G>C , CM000669.1:g.17379388G>C GRCh37
NC_000007.12:g.17345913G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1939G>C MANE Select ENSP00000242057.4:p.Val647Leu
ENST00000637807.1:c.1909G>C ENSP00000490530.1:p.Val637Leu
ENST00000642825.1:c.1894G>C ENSP00000495987.1:p.Val632Leu
ENST00000242057.8:c.1939G>C ENSP00000242057.4:p.Val647Leu
ENST00000463496.1:c.1939G>C ENSP00000436466.1:p.Val647Leu
NM_001621.4:c.1939G>C NP_001612.1:p.Val647Leu
NM_001621.5:c.1939G>C MANE Select NP_001612.1:p.Val647Leu
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