Canonical Allele Identifier: CA561869502
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1322166575
gnomAD v2: 5-110407133-C-T
gnomAD v3: 5-111071435-C-T
gnomAD v4: 5-111071435-C-T
MyVariant Identifiers: chr5:g.110407133C>T (hg19) chr5:g.111071435C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071435C>T , CM000667.2:g.111071435C>T GRCh38
NC_000005.9:g.110407133C>T , CM000667.1:g.110407133C>T GRCh37
NC_000005.8:g.110435032C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-49C>T ENSP00000399099.2:n.-49C>T
NR_045089.1:n.1356C>T
NR_045089.2:n.1374C>T
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