Canonical Allele Identifier: CA1080102128
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752336071

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071469A>G , CM000667.2:g.111071469A>G GRCh38
NC_000005.9:g.110407167A>G , CM000667.1:g.110407167A>G GRCh37
NC_000005.8:g.110435066A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-15A>G ENSP00000399099.2:n.-15A>G
NR_045089.1:n.1390A>G
NR_045089.2:n.1408A>G