Canonical Allele Identifier: CA561869498
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs757611714
gnomAD v2: 5-110407132-C-A
gnomAD v4: 5-111071434-C-A
MyVariant Identifiers: chr5:g.110407132C>A (hg19) chr5:g.111071434C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071434C>A , CM000667.2:g.111071434C>A GRCh38
NC_000005.9:g.110407132C>A , CM000667.1:g.110407132C>A GRCh37
NC_000005.8:g.110435031C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-50C>A ENSP00000399099.2:n.-50C>A
NR_045089.1:n.1355C>A
NR_045089.2:n.1373C>A
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