Canonical Allele Identifier: CA1572616272
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071559A= , CM000667.2:g.111071559A= GRCh38
NC_000005.9:g.110407257A= , CM000667.1:g.110407257A= GRCh37
NC_000005.8:g.110435156A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+42A= ENSP00000399099.2:n.34+42A=
NR_045089.1:n.1438+42A=
NR_045089.2:n.1456+42A=