Canonical Allele Identifier: CA561869515
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1485794874
gnomAD v2: 5-110407157-CG-C
gnomAD v3: 5-111071459-CG-C
gnomAD v4: 5-111071459-CG-C
MyVariant Identifiers: chr5:g.110407158del (hg19) chr5:g.111071460del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071460del , CM000667.2:g.111071460del GRCh38
NC_000005.9:g.110407158del , CM000667.1:g.110407158del GRCh37
NC_000005.8:g.110435057del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-24del ENSP00000399099.2:n.-24del
NR_045089.1:n.1381del
NR_045089.2:n.1399del
Search 100 bp 5'
Search 100 bp 3'