Canonical Allele Identifier: CA801886791
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1183603412
MyVariant Identifiers: chr5:g.110407173T>A (hg19) chr5:g.111071475T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071475T>A , CM000667.2:g.111071475T>A GRCh38
NC_000005.9:g.110407173T>A , CM000667.1:g.110407173T>A GRCh37
NC_000005.8:g.110435072T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-9T>A ENSP00000399099.2:n.-9T>A
NR_045089.1:n.1396T>A
NR_045089.2:n.1414T>A
Search 100 bp 5'
Search 100 bp 3'