Canonical Allele Identifier: CA360602303
Gene: TSLP HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110407188T>A (hg19) chr5:g.111071490T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071490T>A , CM000667.2:g.111071490T>A GRCh38
NC_000005.9:g.110407188T>A , CM000667.1:g.110407188T>A GRCh37
NC_000005.8:g.110435087T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.7T>A ENSP00000399099.2:p.Cys3Ser
NR_045089.1:n.1411T>A
NR_045089.2:n.1429T>A
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