Canonical Allele Identifier: CA2674827781
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071769C>A , CM000667.2:g.111071769C>A GRCh38
NC_000005.9:g.110407467C>A , CM000667.1:g.110407467C>A GRCh37
NC_000005.8:g.110435366C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-122C>A MANE Select ENSP00000339804.3:n.-122C>A
ENST00000344895.3:c.-122C>A ENSP00000339804.3:n.-122C>A
ENST00000420978.6:c.35-156C>A ENSP00000399099.2:n.35-156C>A
NM_033035.4:c.-122C>A NP_149024.1:n.-122C>A
NR_045089.1:n.1439-156C>A
NM_033035.5:c.-122C>A MANE Select NP_149024.1:n.-122C>A
NR_045089.2:n.1457-156C>A