Canonical Allele Identifier: CA454049360
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298424-T-C
MyVariant Identifiers: chr7:g.17338048T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298424T>C , CM000669.2:g.17298424T>C GRCh38
NC_000007.13:g.17338048T>C , CM000669.1:g.17338048T>C GRCh37
NC_000007.12:g.17304573T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1800T>C ENSP00000495987.1:n.20+1800T>C
XR_927069.1:n.113A>G
XR_927070.1:n.113A>G
XR_927071.1:n.113A>G
XR_927072.1:n.114A>G
XR_927073.1:n.115A>G
XR_927073.2:n.115A>G