Canonical Allele Identifier: CA561869514
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs566158190
gnomAD v2: 5-110407157-C-G
gnomAD v3: 5-111071459-C-G
gnomAD v4: 5-111071459-C-G
MyVariant Identifiers: chr5:g.110407157C>G (hg19) chr5:g.111071459C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071459C>G , CM000667.2:g.111071459C>G GRCh38
NC_000005.9:g.110407157C>G , CM000667.1:g.110407157C>G GRCh37
NC_000005.8:g.110435056C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-25C>G ENSP00000399099.2:n.-25C>G
NR_045089.1:n.1380C>G
NR_045089.2:n.1398C>G
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