Canonical Allele Identifier: CA124871398
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs147057210
gnomAD v2: 5-110405786-C-CT
gnomAD v3: 5-111070088-C-CT
gnomAD v4: 5-111070088-C-CT
MyVariant Identifiers: chr5:g.110405786_110405787insT (hg19) chr5:g.111070088_111070089insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111070096dup , CM000667.2:g.111070096dup GRCh38
NC_000005.9:g.110405794dup , CM000667.1:g.110405794dup GRCh37
NC_000005.8:g.110433693dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-1388dup ENSP00000399099.2:n.-1388dup
NR_045089.1:n.17dup
NR_045089.2:n.35dup
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