Canonical Allele Identifier: CA2567096392
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071793T>C , CM000667.2:g.111071793T>C GRCh38
NC_000005.9:g.110407491T>C , CM000667.1:g.110407491T>C GRCh37
NC_000005.8:g.110435390T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-98T>C MANE Select ENSP00000339804.3:n.-98T>C
ENST00000344895.3:c.-98T>C ENSP00000339804.3:n.-98T>C
ENST00000420978.6:c.35-132T>C ENSP00000399099.2:n.35-132T>C
NM_033035.4:c.-98T>C NP_149024.1:n.-98T>C
NR_045089.1:n.1439-132T>C
NM_033035.5:c.-98T>C MANE Select NP_149024.1:n.-98T>C
NR_045089.2:n.1457-132T>C