Canonical Allele Identifier: CA124873571
Gene: TSLP HGNC NCBI

Linked Data

dbSNP Id: rs148498768

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111071983C>G , CM000667.2:g.111071983C>G GRCh38
NC_000005.9:g.110407681C>G , CM000667.1:g.110407681C>G GRCh37
NC_000005.8:g.110435580C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344895.4:c.93C>G MANE Select ENSP00000339804.3:p.Phe31Leu
ENST00000344895.3:c.93C>G ENSP00000339804.3:p.Phe31Leu
ENST00000420978.6:c.93C>G ENSP00000399099.2:p.Phe31Leu
NM_033035.4:c.93C>G NP_149024.1:p.Phe31Leu
NR_045089.1:n.1497C>G
NM_033035.5:c.93C>G MANE Select NP_149024.1:p.Phe31Leu
NR_045089.2:n.1515C>G