Canonical Allele Identifier: CA2674827888
Gene: TSLP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072117C>T , CM000667.2:g.111072117C>T GRCh38
NC_000005.9:g.110407815C>T , CM000667.1:g.110407815C>T GRCh37
NC_000005.8:g.110435714C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.171+56C>T MANE Select ENSP00000339804.3:n.171+56C>T
ENST00000344895.3:c.171+56C>T ENSP00000339804.3:n.171+56C>T
ENST00000420978.6:c.171+56C>T ENSP00000399099.2:n.171+56C>T
NM_033035.4:c.171+56C>T NP_149024.1:n.171+56C>T
NR_045089.1:n.1575+56C>T
NM_033035.5:c.171+56C>T MANE Select NP_149024.1:n.171+56C>T
NR_045089.2:n.1593+56C>T