Canonical Allele Identifier: CA154828313
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs532703285
gnomAD v2: 7-17338060-T-C
gnomAD v3: 7-17298436-T-C
gnomAD v4: 7-17298436-T-C
MyVariant Identifiers: chr7:g.17338060T>C (hg19) chr7:g.17298436T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298436T>C , CM000669.2:g.17298436T>C GRCh38
NC_000007.13:g.17338060T>C , CM000669.1:g.17338060T>C GRCh37
NC_000007.12:g.17304585T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1812T>C ENSP00000495987.1:n.20+1812T>C
XR_927069.1:n.101A>G
XR_927070.1:n.101A>G
XR_927071.1:n.101A>G
XR_927072.1:n.102A>G
XR_927073.1:n.103A>G
XR_927073.2:n.103A>G
Search 100 bp 5'
Search 100 bp 3'