Canonical Allele Identifier: CA124874225
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs10062929

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111072481C>A , CM000667.2:g.111072481C>A GRCh38
NC_000005.9:g.110408179C>A , CM000667.1:g.110408179C>A GRCh37
NC_000005.8:g.110436078C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344895.4:c.172-407C>A MANE Select ENSP00000339804.3:p.=
ENST00000344895.3:c.172-407C>A ENSP00000339804.3:p.=
ENST00000420978.6:c.172-407C>A ENSP00000399099.2:p.=
NM_033035.4:c.172-407C>A NP_149024.1:p.=
NR_045089.1:n.1576-407C>A
NM_033035.5:c.172-407C>A MANE Select NP_149024.1:p.=
NR_045089.2:n.1594-407C>A