Canonical Allele Identifier: CA2681907564
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17247569-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247569T>C , CM000669.2:g.17247569T>C GRCh38
NC_000007.13:g.17287193T>C , CM000669.1:g.17287193T>C GRCh37
NC_000007.12:g.17253718T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-360T>C ENSP00000495987.1:n.-360T>C
XR_927073.2:n.861+11683A>G