Canonical Allele Identifier: CA561869566
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1233442496
gnomAD v2: 5-110407342-C-A
gnomAD v3: 5-111071644-C-A
gnomAD v4: 5-111071644-C-A
MyVariant Identifiers: chr5:g.110407342C>A (hg19) chr5:g.111071644C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071644C>A , CM000667.2:g.111071644C>A GRCh38
NC_000005.9:g.110407342C>A , CM000667.1:g.110407342C>A GRCh37
NC_000005.8:g.110435241C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+127C>A ENSP00000399099.2:n.34+127C>A
NR_045089.1:n.1438+127C>A
NR_045089.2:n.1456+127C>A
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