Canonical Allele Identifier: CA2674827648
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071602A>C , CM000667.2:g.111071602A>C GRCh38
NC_000005.9:g.110407300A>C , CM000667.1:g.110407300A>C GRCh37
NC_000005.8:g.110435199A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+85A>C ENSP00000399099.2:n.34+85A>C
NR_045089.1:n.1438+85A>C
NR_045089.2:n.1456+85A>C