Canonical Allele Identifier: CA651081509
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1300513219
gnomAD v4: 7-17298524-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298524G>C , CM000669.2:g.17298524G>C GRCh38
NC_000007.13:g.17338148G>C , CM000669.1:g.17338148G>C GRCh37
NC_000007.12:g.17304673G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1900G>C ENSP00000495987.1:n.20+1900G>C
XR_927069.1:n.13C>G
XR_927070.1:n.13C>G
XR_927071.1:n.13C>G
XR_927072.1:n.14C>G
XR_927073.1:n.15C>G
XR_927073.2:n.15C>G