Canonical Allele Identifier: CA124873152
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs965270845

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071703G>C , CM000667.2:g.111071703G>C GRCh38
NC_000005.9:g.110407401G>C , CM000667.1:g.110407401G>C GRCh37
NC_000005.8:g.110435300G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.3:c.-188G>C ENSP00000339804.3:n.-188G>C
ENST00000420978.6:c.34+186G>C ENSP00000399099.2:n.34+186G>C
NM_033035.4:c.-188G>C NP_149024.1:n.-188G>C
NR_045089.1:n.1438+186G>C
NR_045089.2:n.1456+186G>C