Canonical Allele Identifier: CA2674827759
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071741G>T , CM000667.2:g.111071741G>T GRCh38
NC_000005.9:g.110407439G>T , CM000667.1:g.110407439G>T GRCh37
NC_000005.8:g.110435338G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.-150G>T MANE Select ENSP00000339804.3:n.-150G>T
ENST00000344895.3:c.-150G>T ENSP00000339804.3:n.-150G>T
ENST00000420978.6:c.35-184G>T ENSP00000399099.2:n.35-184G>T
NM_033035.4:c.-150G>T NP_149024.1:n.-150G>T
NR_045089.1:n.1439-184G>T
NM_033035.5:c.-150G>T MANE Select NP_149024.1:n.-150G>T
NR_045089.2:n.1457-184G>T