Canonical Allele Identifier: CA801886970
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1200756986

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071680G>T , CM000667.2:g.111071680G>T GRCh38
NC_000005.9:g.110407378G>T , CM000667.1:g.110407378G>T GRCh37
NC_000005.8:g.110435277G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+163G>T ENSP00000399099.2:n.34+163G>T
NR_045089.1:n.1438+163G>T
NR_045089.2:n.1456+163G>T