Canonical Allele Identifier: CA561869557
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752339242
gnomAD v2: 5-110407286-C-CTTTTTTT
MyVariant Identifiers: chr5:g.110407286_110407287insTTTTTTT (hg19) chr5:g.111071588_111071589insTTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071591_111071592insTTTTTTT , CM000667.2:g.111071591_111071592insTTTTTTT GRCh38
NC_000005.9:g.110407289_110407290insTTTTTTT , CM000667.1:g.110407289_110407290insTTTTTTT GRCh37
NC_000005.8:g.110435188_110435189insTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+74_34+75insTTTTTTT ENSP00000399099.2:n.34+74_34+75insTTTTTTT
NR_045089.1:n.1438+74_1438+75insTTTTTTT
NR_045089.2:n.1456+74_1456+75insTTTTTTT
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