Canonical Allele Identifier: CA561869541
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1237168159

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071547T>C , CM000667.2:g.111071547T>C GRCh38
NC_000005.9:g.110407245T>C , CM000667.1:g.110407245T>C GRCh37
NC_000005.8:g.110435144T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+30T>C ENSP00000399099.2:n.34+30T>C
NR_045089.1:n.1438+30T>C
NR_045089.2:n.1456+30T>C