Canonical Allele Identifier: CA12103925
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs2289276

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071809C>T , CM000667.2:g.111071809C>T GRCh38
NC_000005.9:g.110407507C>T , CM000667.1:g.110407507C>T GRCh37
NC_000005.8:g.110435406C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.-82C>T MANE Select ENSP00000339804.3:p.=
ENST00000344895.3:c.-82C>T ENSP00000339804.3:p.=
ENST00000420978.6:c.35-116C>T ENSP00000399099.2:p.=
NM_033035.4:c.-82C>T NP_149024.1:p.=
NR_045089.1:n.1439-116C>T
NM_033035.5:c.-82C>T MANE Select NP_149024.1:p.=
NR_045089.2:n.1457-116C>T