Canonical Allele Identifier: CA12103924
Gene: TSLP HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.111071044C>T
GRCh37 chr5:g.110406742C>T
gnomAD v2:
5:110406742 C / T
gnomAD v3:
5:111071044 C / T
gnomAD v4:
chr5-111071044-C-T
Joint Max Group AF 0.64578445 (SAS)
Genomes Max Group AF 0.64477722 (SAS)
Exomes Max Group AF 0.58301959 (SAS)
dbSNP:
3806933
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071044C>T , CM000667.2:g.111071044C>T GRCh38
NC_000005.9:g.110406742C>T , CM000667.1:g.110406742C>T GRCh37
NC_000005.8:g.110434641C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-440C>T ENSP00000399099.2:n.-440C>T
NR_045089.1:n.965C>T
NR_045089.2:n.983C>T
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