Canonical Allele Identifier: CA2681909918
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339839-TATA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339842_17339844del , CM000669.2:g.17339842_17339844del GRCh38
NC_000007.13:g.17379466_17379468del , CM000669.1:g.17379466_17379468del GRCh37
NC_000007.12:g.17345991_17345993del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2017_2019del MANE Select ENSP00000242057.4:p.Asn673del
ENST00000637807.1:c.1987_1989del ENSP00000490530.1:p.Asn663del
ENST00000642825.1:c.1972_1974del ENSP00000495987.1:p.Asn658del
ENST00000242057.8:c.2017_2019del ENSP00000242057.4:p.Asn673del
ENST00000463496.1:c.2017_2019del ENSP00000436466.1:p.Asn673del
NM_001621.4:c.2017_2019del NP_001612.1:p.Asn673del
NM_001621.5:c.2017_2019del MANE Select NP_001612.1:p.Asn673del
Search 100 bp 5'
Search 100 bp 3'