Canonical Allele Identifier: CA124873079
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs535116768

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071635G>A , CM000667.2:g.111071635G>A GRCh38
NC_000005.9:g.110407333G>A , CM000667.1:g.110407333G>A GRCh37
NC_000005.8:g.110435232G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+118G>A ENSP00000399099.2:n.34+118G>A
NR_045089.1:n.1438+118G>A
NR_045089.2:n.1456+118G>A