Canonical Allele Identifier: CA561869519
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1269053792
gnomAD v2: 5-110407161-T-C
gnomAD v4: 5-111071463-T-C
MyVariant Identifiers: chr5:g.110407161T>C (hg19) chr5:g.111071463T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071463T>C , CM000667.2:g.111071463T>C GRCh38
NC_000005.9:g.110407161T>C , CM000667.1:g.110407161T>C GRCh37
NC_000005.8:g.110435060T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-21T>C ENSP00000399099.2:n.-21T>C
NR_045089.1:n.1384T>C
NR_045089.2:n.1402T>C
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