Canonical Allele Identifier: CA801886969
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1396853668
gnomAD v3: 5-111071676-T-G
gnomAD v4: 5-111071676-T-G
MyVariant Identifiers: chr5:g.110407374T>G (hg19) chr5:g.111071676T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071676T>G , CM000667.2:g.111071676T>G GRCh38
NC_000005.9:g.110407374T>G , CM000667.1:g.110407374T>G GRCh37
NC_000005.8:g.110435273T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+159T>G ENSP00000399099.2:n.34+159T>G
NR_045089.1:n.1438+159T>G
NR_045089.2:n.1456+159T>G
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