Canonical Allele Identifier: CA366895646
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339806C>T , CM000669.2:g.17339806C>T GRCh38
NC_000007.13:g.17379430C>T , CM000669.1:g.17379430C>T GRCh37
NC_000007.12:g.17345955C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1981C>T MANE Select ENSP00000242057.4:p.Pro661Ser
ENST00000637807.1:c.1951C>T ENSP00000490530.1:p.Pro651Ser
ENST00000642825.1:c.1936C>T ENSP00000495987.1:p.Pro646Ser
ENST00000242057.8:c.1981C>T ENSP00000242057.4:p.Pro661Ser
ENST00000463496.1:c.1981C>T ENSP00000436466.1:p.Pro661Ser
NM_001621.4:c.1981C>T NP_001612.1:p.Pro661Ser
NM_001621.5:c.1981C>T MANE Select NP_001612.1:p.Pro661Ser