Canonical Allele Identifier: CA2681911142
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298529-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298529G>T , CM000669.2:g.17298529G>T GRCh38
NC_000007.13:g.17338153G>T , CM000669.1:g.17338153G>T GRCh37
NC_000007.12:g.17304678G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1905G>T ENSP00000495987.1:n.20+1905G>T
XR_927069.1:n.8C>A
XR_927070.1:n.8C>A
XR_927071.1:n.8C>A
XR_927072.1:n.9C>A
XR_927073.1:n.10C>A
XR_927073.2:n.10C>A