Canonical Allele Identifier: CA154827736

Gene: AHR

Linked Data

• dbSNP Id: rs912919096
• gnomAD v2: 7-17332912-CT-C
• gnomAD v3: 7-17293288-CT-C
• gnomAD v4: 7-17293288-CT-C
• MyVariant Identifiers: chr7:g.17332913del (hg19) ; chr7:g.17293289del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293298del , CM000669.2:g.17293298del	GRCh38
NC_000007.13:g.17332922del , CM000669.1:g.17332922del	GRCh37
NC_000007.12:g.17299447del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2999del	ENSP00000495987.1:n.-202-2999del
XR_927069.1:n.293+1877del
XR_927070.1:n.293+1877del
XR_927071.1:n.293+1877del
XR_927072.1:n.294+1877del
XR_927073.1:n.295+1877del
XR_927073.2:n.295+1877del