Canonical Allele Identifier: CA1080102131
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs1752336576

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071480A>T , CM000667.2:g.111071480A>T GRCh38
NC_000005.9:g.110407178A>T , CM000667.1:g.110407178A>T GRCh37
NC_000005.8:g.110435077A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420978.6:c.-4A>T ENSP00000399099.2:n.-4A>T
NR_045089.1:n.1401A>T
NR_045089.2:n.1419A>T