Canonical Allele Identifier: CA1572617149
Gene: TSLP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072256G= , CM000667.2:g.111072256G= GRCh38
NC_000005.9:g.110407954G= , CM000667.1:g.110407954G= GRCh37
NC_000005.8:g.110435853G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.171+195G= MANE Select ENSP00000339804.3:n.171+195G=
ENST00000344895.3:c.171+195G= ENSP00000339804.3:n.171+195G=
ENST00000420978.6:c.171+195G= ENSP00000399099.2:n.171+195G=
NM_033035.4:c.171+195G= NP_149024.1:n.171+195G=
NR_045089.1:n.1575+195G=
NM_033035.5:c.171+195G= MANE Select NP_149024.1:n.171+195G=
NR_045089.2:n.1593+195G=