Canonical Allele Identifier: CA124872856
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs991309232

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071413A>G , CM000667.2:g.111071413A>G GRCh38
NC_000005.9:g.110407111A>G , CM000667.1:g.110407111A>G GRCh37
NC_000005.8:g.110435010A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-71A>G ENSP00000399099.2:n.-71A>G
NR_045089.1:n.1334A>G
NR_045089.2:n.1352A>G