Canonical Allele Identifier: CA561869517
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs137996521
gnomAD v2: 5-110407158-G-C
gnomAD v3: 5-111071460-G-C
gnomAD v4: 5-111071460-G-C
MyVariant Identifiers: chr5:g.110407158G>C (hg19) chr5:g.111071460G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071460G>C , CM000667.2:g.111071460G>C GRCh38
NC_000005.9:g.110407158G>C , CM000667.1:g.110407158G>C GRCh37
NC_000005.8:g.110435057G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-24G>C ENSP00000399099.2:n.-24G>C
NR_045089.1:n.1381G>C
NR_045089.2:n.1399G>C
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