Canonical Allele Identifier: CA561869560
Gene: TSLP HGNC NCBI

Linked Data

gnomAD v2: 5-110407286-C-CTTT
gnomAD v3: 5-111071588-C-CTTT
gnomAD v4: 5-111071588-C-CTTT
MyVariant Identifiers: chr5:g.110407286_110407287insTTT (hg19) chr5:g.111071588_111071589insTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071589_111071591dup , CM000667.2:g.111071589_111071591dup GRCh38
NC_000005.9:g.110407287_110407289dup , CM000667.1:g.110407287_110407289dup GRCh37
NC_000005.8:g.110435186_110435188dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+72_34+74dup ENSP00000399099.2:n.34+72_34+74dup
NR_045089.1:n.1438+72_1438+74dup
NR_045089.2:n.1456+72_1456+74dup
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