Canonical Allele Identifier: CA561869520
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1464497322
gnomAD v2: 5-110407176-A-T
gnomAD v4: 5-111071478-A-T
MyVariant Identifiers: chr5:g.110407176A>T (hg19) chr5:g.111071478A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071478A>T , CM000667.2:g.111071478A>T GRCh38
NC_000005.9:g.110407176A>T , CM000667.1:g.110407176A>T GRCh37
NC_000005.8:g.110435075A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-6A>T ENSP00000399099.2:n.-6A>T
NR_045089.1:n.1399A>T
NR_045089.2:n.1417A>T
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