Canonical Allele Identifier: CA561869522
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1203530657
gnomAD v2: 5-110407178-A-AT
gnomAD v4: 5-111071480-A-AT
MyVariant Identifiers: chr5:g.110407178_110407179insT (hg19) chr5:g.111071480_111071481insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071480_111071481insT , CM000667.2:g.111071480_111071481insT GRCh38
NC_000005.9:g.110407178_110407179insT , CM000667.1:g.110407178_110407179insT GRCh37
NC_000005.8:g.110435077_110435078insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-4_-3insT ENSP00000399099.2:n.-4_-3insT
NR_045089.1:n.1401_1402insT
NR_045089.2:n.1419_1420insT
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