Canonical Allele Identifier: CA124872815
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs560975805
gnomAD v3: 5-111071403-C-A
gnomAD v4: 5-111071403-C-A
MyVariant Identifiers: chr5:g.110407101C>A (hg19) chr5:g.111071403C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071403C>A , CM000667.2:g.111071403C>A GRCh38
NC_000005.9:g.110407101C>A , CM000667.1:g.110407101C>A GRCh37
NC_000005.8:g.110435000C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-81C>A ENSP00000399099.2:n.-81C>A
NR_045089.1:n.1324C>A
NR_045089.2:n.1342C>A
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