Canonical Allele Identifier: CA1572616269
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752338591

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071554A>G , CM000667.2:g.111071554A>G GRCh38
NC_000005.9:g.110407252A>G , CM000667.1:g.110407252A>G GRCh37
NC_000005.8:g.110435151A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.34+37A>G ENSP00000399099.2:n.34+37A>G
NR_045089.1:n.1438+37A>G
NR_045089.2:n.1456+37A>G